rs_ID |
Location |
Functional Annotation |
rs9993599 |
Chr4:56452965(Fwd) |
intron_variant |
rs11726287 |
Chr4:6423198(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10155282 |
Chr4:814719(Fwd) |
intron_variant |
rs2171022 |
Chr4:168181071(Fwd) |
|
rs6842960 |
Chr4:56456154(Fwd) |
intron_variant |
rs17778826 |
Chr4:6425308(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7377207 |
Chr4:815107(Fwd) |
intron_variant |
rs7660952 |
Chr4:91830371(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10021233 |
Chr4:56239822(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4689002 |
Chr4:6427972(Fwd) |
intron_variant; nc_transcript_variant |
rs1078139 |
Chr4:828148(Fwd) |
downstream_gene_variant |
rs7683403 |
Chr4:91830465(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs552792 |
Chr4:56246273(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4689443 |
Chr4:6429992(Fwd) |
intron_variant; nc_transcript_variant |
rs2127168 |
Chr4:830601(Fwd) |
nc_transcript_variant; non_coding_exon_variant |
rs7683238 |
Chr4:91830496(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs693367 |
Chr4:56260662(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs744699 |
Chr4:6430773(Fwd) |
intron_variant; nc_transcript_variant |
rs8093 |
Chr4:843695(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
rs6855137 |
Chr4:91832609(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs3792603 |
Chr4:56302058(Fwd) |
intron_variant; nc_transcript_variant |
rs4334819 |
Chr4:6431416(Fwd) |
intron_variant; nc_transcript_variant |
rs2306248 |
Chr4:860146(Fwd) |
intron_variant; nc_transcript_variant; splice_region_variant |
rs11722502 |
Chr4:22556784(Fwd) |
|
rs11932595 |
Chr4:56323597(Fwd) |
intron_variant; nc_transcript_variant |
rs11724762 |
Chr4:6433905(Fwd) |
intron_variant; nc_transcript_variant |
rs4690332 |
Chr4:910520(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2323549 |
Chr4:22579261(Fwd) |
|
rs7659095 |
Chr4:56401601(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12507333 |
Chr4:6435379(Fwd) |
intron_variant; nc_transcript_variant |
rs7663192 |
Chr4:923947(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs13101950 |
Chr4:22533398(Fwd) |
|
rs13434995 |
Chr4:56467214(Fwd) |
intron_variant; nc_transcript_variant |
rs4522940 |
Chr4:6438660(Fwd) |
intron_variant; nc_transcript_variant |
rs10026861 |
Chr4:22538841(Fwd) |
|
rs9996936 |
Chr4:56467639(Fwd) |
intron_variant; nc_transcript_variant |
rs9991896 |
Chr4:6444182(Fwd) |
intron_variant; nc_transcript_variant |
rs10027019 |
Chr4:22538956(Fwd) |
|
rs10018932 |
Chr4:56467866(Fwd) |
intron_variant; nc_transcript_variant |
rs12645522 |
Chr4:20856831(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1841829 |
Chr4:22546306(Fwd) |
|
rs10011801 |
Chr4:56468734(Fwd) |
intron_variant; nc_transcript_variant |
rs1158971 |
Chr4:20866586(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2875050 |
Chr4:22551798(Fwd) |
|
rs10000512 |
Chr4:56469022(Fwd) |
intron_variant; nc_transcript_variant |
rs7694587 |
Chr4:20850880(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2323438 |
Chr4:22554923(Fwd) |
|
rs1873091 |
Chr4:56471433(Fwd) |
intron_variant; nc_transcript_variant |
rs7673250 |
Chr4:20850986(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2323623 |
Chr4:22559185(Fwd) |
|
rs17725110 |
Chr4:56472022(Fwd) |
intron_variant; nc_transcript_variant |
rs4697193 |
Chr4:20851191(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10938910 |
Chr4:22572864(Fwd) |
|
rs3805383 |
Chr4:56475338(Fwd) |
nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
rs3765119 |
Chr4:20851969(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs2323550 |
Chr4:22579076(Fwd) |
|
rs17725163 |
Chr4:56475447(Fwd) |
intron_variant; nc_transcript_variant |
rs3765120 |
Chr4:20852001(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs6838277 |
Chr4:22581096(Fwd) |
|
rs10026315 |
Chr4:56478362(Fwd) |
intron_variant; nc_transcript_variant |
rs3765121 |
Chr4:20852166(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant; splice_region_variant; synonymous_variant |
rs6843786 |
Chr4:22587351(Fwd) |
|
rs10026676 |
Chr4:56478752(Fwd) |
intron_variant; nc_transcript_variant |
rs3765122 |
Chr4:20852244(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
rs6811994 |
Chr4:22526601(Fwd) |
|
rs17781708 |
Chr4:56481069(Fwd) |
intron_variant; nc_transcript_variant |
rs10938811 |
Chr4:20853065(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7680019 |
Chr4:22556585(Fwd) |
|
rs3805389 |
Chr4:56482750(Fwd) |
intron_variant; nc_transcript_variant |
rs2874862 |
Chr4:20853751(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10938913 |
Chr4:22584439(Fwd) |
|
rs819266 |
Chr4:56235592(Fwd) |
intron_variant; nc_transcript_variant |
rs7669354 |
Chr4:20854588(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17601963 |
Chr4:22586532(Fwd) |
|
rs576732 |
Chr4:56237137(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7669387 |
Chr4:20854640(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2045814 |
Chr4:22543823(Fwd) |
|
rs6858749 |
Chr4:56290437(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs11732723 |
Chr4:56290558(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs1844812 |
Chr4:20856032(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs819268 |
Chr4:56235931(Fwd) |
intron_variant; nc_transcript_variant |
rs10938814 |
Chr4:20856297(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2538 |
Chr4:56236328(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10517549 |
Chr4:62789268(Fwd) |
intron_variant |
rs10938815 |
Chr4:20856353(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs819270 |
Chr4:56238626(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10023425 |
Chr4:62788474(Fwd) |
intron_variant |
rs12505671 |
Chr4:20857040(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11943456 |
Chr4:56276334(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11131347 |
Chr4:62759270(Fwd) |
intron_variant; upstream_gene_variant |
rs9291413 |
Chr4:20861032(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs819269 |
Chr4:56238263(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1376309 |
Chr4:62762646(Fwd) |
intron_variant |
rs1388321 |
Chr4:20880744(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1450900 |
Chr4:62763217(Fwd) |
intron_variant |
rs6551666 |
Chr4:62763475(Fwd) |
intron_variant |
rs5012949 |
Chr4:62763822(Fwd) |
intron_variant |
rs7695892 |
Chr4:62765438(Fwd) |
intron_variant |
rs1376310 |
Chr4:62765983(Fwd) |
intron_variant |
rs7690962 |
Chr4:62766992(Fwd) |
intron_variant |
rs10020948 |
Chr4:62767097(Fwd) |
intron_variant; upstream_gene_variant |
rs6813183 |
Chr4:62769131(Fwd) |
intron_variant; upstream_gene_variant |
rs6551669 |
Chr4:62770893(Fwd) |
intron_variant; upstream_gene_variant |
rs4860442 |
Chr4:62773995(Fwd) |
downstream_gene_variant; intron_variant |
rs12503398 |
Chr4:62778315(Fwd) |
intron_variant |
rs13152451 |
Chr4:6425624(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1510925 |
Chr4:62830533(Fwd) |
intron_variant |
rs4345249 |
Chr4:6427070(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1397543 |
Chr4:62839065(Fwd) |
intron_variant |
rs17722973 |
Chr4:6441415(Fwd) |
intron_variant; nc_transcript_variant |
rs10030755 |
Chr4:62844408(Fwd) |
intron_variant |
rs6829169 |
Chr4:6441967(Fwd) |
intron_variant; nc_transcript_variant |
rs1470724 |
Chr4:62761870(Fwd) |
intron_variant |
rs6813956 |
Chr4:6442931(Fwd) |
intron_variant; nc_transcript_variant |
rs1349408 |
Chr4:62766445(Fwd) |
intron_variant |
rs16835101 |
Chr4:6443045(Fwd) |
intron_variant; nc_transcript_variant |
rs6843396 |
Chr4:62775733(Fwd) |
downstream_gene_variant; intron_variant |
rs10032537 |
Chr4:20698104(Fwd) |
5_prime_UTR_variant; NMD_transcript_variant; upstream_gene_variant |
rs4690281 |
Chr4:753944(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7688805 |
Chr4:20732334(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2242233 |
Chr4:755025(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10516360 |
Chr4:20704340(Fwd) |
5_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs899393 |
Chr4:758366(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs7679050 |
Chr4:20707821(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs4690194 |
Chr4:760819(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12331962 |
Chr4:20714769(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs11248040 |
Chr4:770508(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs9291412 |
Chr4:20727464(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17165034 |
Chr4:798962(Fwd) |
intron_variant; upstream_gene_variant |
rs10024417 |
Chr4:20660406(Fwd) |
|
rs4690307 |
Chr4:755749(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs10516359 |
Chr4:20675834(Fwd) |
|
rs17165032 |
Chr4:798817(Fwd) |
intron_variant; upstream_gene_variant |
rs11727810 |
Chr4:20675848(Fwd) |
|
rs4690282 |
Chr4:754484(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs28414076 |
Chr4:20676535(Fwd) |
|
rs10026509 |
Chr4:20696120(Fwd) |
upstream_gene_variant |
rs13101486 |
Chr4:21306185(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs983071 |
Chr4:21306814(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs13108702 |
Chr4:21307087(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs13120431 |
Chr4:21312027(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12643751 |
Chr4:21316608(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2007762 |
Chr4:21301546(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs11734360 |
Chr4:21310634(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs13108412 |
Chr4:21314195(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs13118906 |
Chr4:21317300(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4696975 |
Chr4:21318171(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs17226342 |
Chr4:62817231(Fwd) |
downstream_gene_variant; intron_variant |
rs11932133 |
Chr4:95792794(Fwd) |
intron_variant |
rs995447 |
Chr4:62818468(Fwd) |
intron_variant |
rs17022403 |
Chr4:95791533(Fwd) |
intron_variant |
rs989295 |
Chr4:62821189(Fwd) |
intron_variant |
rs3775005 |
Chr4:95798592(Fwd) |
intron_variant |
rs4860446 |
Chr4:62826705(Fwd) |
intron_variant |
rs13105913 |
Chr4:95804237(Fwd) |
intron_variant |
rs7672853 |
Chr4:62838634(Fwd) |
intron_variant |
rs739729 |
Chr4:95804508(Fwd) |
intron_variant |
rs12649738 |
Chr4:62840086(Fwd) |
intron_variant |
rs1011959 |
Chr4:95809725(Fwd) |
intron_variant |
rs7437338 |
Chr4:62765805(Fwd) |
intron_variant |
rs1011961 |
Chr4:95810540(Fwd) |
intron_variant |
rs970358 |
Chr4:62781230(Fwd) |
intron_variant |
rs6820744 |
Chr4:95811080(Fwd) |
intron_variant |
rs1450894 |
Chr4:62786077(Fwd) |
intron_variant |
rs1541372 |
Chr4:95812175(Fwd) |
intron_variant |
rs10517550 |
Chr4:62797069(Fwd) |
intron_variant; upstream_gene_variant |
rs17022471 |
Chr4:95812220(Fwd) |
intron_variant |
rs4386675 |
Chr4:6351958(Fwd) |
intron_variant; nc_transcript_variant |
rs10027079 |
Chr4:62812447(Fwd) |
intron_variant; nc_transcript_variant |
rs17022477 |
Chr4:95812743(Fwd) |
intron_variant |
rs11730177 |
Chr4:6356513(Fwd) |
intron_variant; nc_transcript_variant |
rs10031103 |
Chr4:62823530(Fwd) |
intron_variant |
rs17501058 |
Chr4:95815162(Fwd) |
intron_variant |
rs11727834 |
Chr4:6352274(Fwd) |
intron_variant; nc_transcript_variant |
rs10008326 |
Chr4:62823663(Fwd) |
intron_variant |
rs17429196 |
Chr4:95817017(Fwd) |
intron_variant |
rs13124487 |
Chr4:6364311(Fwd) |
intron_variant; nc_transcript_variant |
rs12505782 |
Chr4:62833658(Fwd) |
intron_variant |
rs3775009 |
Chr4:95821404(Fwd) |
intron_variant |
rs11734877 |
Chr4:177123630(Fwd) |
|
rs1510923 |
Chr4:62834741(Fwd) |
intron_variant |
rs17429252 |
Chr4:95821655(Fwd) |
intron_variant |
rs1158472 |
Chr4:177128425(Fwd) |
|
rs1397544 |
Chr4:62835493(Fwd) |
intron_variant |
rs6816886 |
Chr4:95822524(Fwd) |
intron_variant |
rs17672480 |
Chr4:177128689(Fwd) |
|
rs7667199 |
Chr4:62840940(Fwd) |
intron_variant |
rs6849640 |
Chr4:95823682(Fwd) |
intron_variant |
rs6832177 |
Chr4:177113836(Fwd) |
downstream_gene_variant; synonymous_variant |
rs1355368 |
Chr4:62779822(Fwd) |
intron_variant |
rs7698986 |
Chr4:95825114(Fwd) |
intron_variant |
rs17062599 |
Chr4:177119115(Fwd) |
upstream_gene_variant |
rs6843945 |
Chr4:62791716(Fwd) |
intron_variant |
rs17429308 |
Chr4:95831071(Fwd) |
intron_variant |
rs10004686 |
Chr4:177120026(Fwd) |
upstream_gene_variant |
rs2122646 |
Chr4:62796294(Fwd) |
intron_variant; upstream_gene_variant |
rs2240036 |
Chr4:95831420(Fwd) |
intron_variant |
rs7686009 |
Chr4:177120728(Fwd) |
upstream_gene_variant |
rs17082493 |
Chr4:62799629(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs1444933 |
Chr4:95835442(Fwd) |
intron_variant |
rs728846 |
Chr4:177121983(Fwd) |
|
rs7690226 |
Chr4:95838109(Fwd) |
intron_variant |
rs11932660 |
Chr4:95838719(Fwd) |
intron_variant |
rs17022573 |
Chr4:95840890(Fwd) |
intron_variant |
rs13133713 |
Chr4:95840995(Fwd) |
intron_variant |
rs3775016 |
Chr4:95841925(Fwd) |
intron_variant |
rs6826498 |
Chr4:22139481(Fwd) |
intron_variant; nc_transcript_variant |
rs7669822 |
Chr4:95841960(Fwd) |
intron_variant |
rs11728484 |
Chr4:22163667(Fwd) |
intron_variant; nc_transcript_variant |
rs2044327 |
Chr4:95845241(Fwd) |
intron_variant |
rs7669791 |
Chr4:22098821(Fwd) |
intron_variant; nc_transcript_variant |
rs10213566 |
Chr4:95829907(Fwd) |
intron_variant |
rs10019171 |
Chr4:22107318(Fwd) |
intron_variant; nc_transcript_variant |
rs972409 |
Chr4:95832551(Fwd) |
intron_variant |
rs2345049 |
Chr4:62637158(Fwd) |
downstream_gene_variant; intron_variant |
rs6818210 |
Chr4:22109914(Fwd) |
intron_variant; nc_transcript_variant |
rs739730 |
Chr4:95805242(Fwd) |
intron_variant |
rs2345047 |
Chr4:62638468(Fwd) |
downstream_gene_variant; intron_variant |
rs4697267 |
Chr4:22111275(Fwd) |
intron_variant; nc_transcript_variant |
rs3775010 |
Chr4:95821419(Fwd) |
intron_variant |
rs10015258 |
Chr4:62642444(Fwd) |
intron_variant; upstream_gene_variant |
rs16872408 |
Chr4:22114968(Fwd) |
intron_variant; nc_transcript_variant |
rs17022547 |
Chr4:95832319(Fwd) |
intron_variant |
rs2345045 |
Chr4:62647220(Fwd) |
intron_variant |
rs17528275 |
Chr4:22124060(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7661079 |
Chr4:95836744(Fwd) |
intron_variant |
rs2345044 |
Chr4:62647756(Fwd) |
intron_variant |
rs7664665 |
Chr4:22126141(Fwd) |
intron_variant; nc_transcript_variant |
rs3821962 |
Chr4:95845632(Fwd) |
intron_variant |
rs2345043 |
Chr4:62647908(Fwd) |
intron_variant |
rs4410519 |
Chr4:22139464(Fwd) |
intron_variant; nc_transcript_variant |
rs3775023 |
Chr4:95846962(Fwd) |
intron_variant |
rs4493573 |
Chr4:62665721(Fwd) |
intron_variant |
rs4334741 |
Chr4:22159445(Fwd) |
intron_variant; nc_transcript_variant |
rs3775028 |
Chr4:95855345(Fwd) |
intron_variant |
rs7656882 |
Chr4:62680775(Fwd) |
intron_variant |
rs2323308 |
Chr4:22086194(Fwd) |
intron_variant; nc_transcript_variant |
rs1376307 |
Chr4:62688669(Fwd) |
intron_variant |
rs11933151 |
Chr4:22164317(Fwd) |
intron_variant; nc_transcript_variant |
rs1901220 |
Chr4:62651861(Fwd) |
intron_variant |
rs17633333 |
Chr4:166926573(Fwd) |
NMD_transcript_variant; intron_variant |
rs17689892 |
Chr4:166927050(Fwd) |
NMD_transcript_variant; intron_variant |
rs17689964 |
Chr4:166946775(Fwd) |
NMD_transcript_variant; intron_variant |
rs17633422 |
Chr4:166948998(Fwd) |
NMD_transcript_variant; intron_variant |
rs1393857 |
Chr4:166933791(Fwd) |
NMD_transcript_variant; intron_variant |
rs9884923 |
Chr4:21719296(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10034603 |
Chr4:21729953(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs10012747 |
Chr4:21730447(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs6448069 |
Chr4:21734198(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6551645 |
Chr4:62573803(Fwd) |
intron_variant |
rs7378252 |
Chr4:21734789(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17090543 |
Chr4:62680962(Fwd) |
intron_variant |
rs4585337 |
Chr4:62595456(Fwd) |
intron_variant |
rs6448072 |
Chr4:21743231(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2881027 |
Chr4:62685720(Fwd) |
intron_variant |
rs7678046 |
Chr4:62596693(Fwd) |
intron_variant |
rs9291430 |
Chr4:21745448(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs9942184 |
Chr4:62692439(Fwd) |
intron_variant |
rs12649170 |
Chr4:62575631(Fwd) |
intron_variant |
rs6448075 |
Chr4:21752712(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11734607 |
Chr4:62693692(Fwd) |
intron_variant |
rs4283700 |
Chr4:62579087(Fwd) |
intron_variant |
rs1459274 |
Chr4:21753319(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12509742 |
Chr4:62645032(Fwd) |
intron_variant; upstream_gene_variant |
rs10022833 |
Chr4:62582072(Fwd) |
intron_variant |
rs2018175 |
Chr4:21754408(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4860434 |
Chr4:62655728(Fwd) |
intron_variant |
rs7670950 |
Chr4:62582865(Fwd) |
intron_variant |
rs1380270 |
Chr4:21755399(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1901223 |
Chr4:62660731(Fwd) |
intron_variant |
rs4860428 |
Chr4:62585313(Fwd) |
intron_variant |
rs10031539 |
Chr4:21759229(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1817052 |
Chr4:62666863(Fwd) |
intron_variant |
rs10021572 |
Chr4:62586113(Fwd) |
intron_variant |
rs6856781 |
Chr4:21759766(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2013374 |
Chr4:62697760(Fwd) |
intron_variant |
rs9998713 |
Chr4:62586313(Fwd) |
intron_variant |
rs17498679 |
Chr4:21761746(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2122642 |
Chr4:62698264(Fwd) |
intron_variant |
rs7684100 |
Chr4:62590133(Fwd) |
intron_variant |
rs17498715 |
Chr4:21762186(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2345041 |
Chr4:62698357(Fwd) |
intron_variant |
rs6840548 |
Chr4:62590297(Fwd) |
intron_variant |
rs17017347 |
Chr4:91573596(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1809267 |
Chr4:21768895(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs990640 |
Chr4:62698937(Fwd) |
intron_variant |
rs1510918 |
Chr4:62859889(Fwd) |
intron_variant |
rs9997427 |
Chr4:62591014(Fwd) |
intron_variant |
rs1399408 |
Chr4:91575934(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1562815 |
Chr4:21769253(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6845019 |
Chr4:62701222(Fwd) |
intron_variant |
rs2271338 |
Chr4:62862251(Fwd) |
intron_variant |
rs5525 |
Chr4:149356516(Fwd) |
synonymous_variant |
rs4312783 |
Chr4:62594187(Fwd) |
intron_variant |
rs1039149 |
Chr4:91580312(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs35609084 |
Chr4:21769939(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2122640 |
Chr4:62654115(Fwd) |
intron_variant |
rs2248038 |
Chr4:149364999(Fwd) |
intron_variant; upstream_gene_variant |
rs6551637 |
Chr4:62502358(Fwd) |
intron_variant; nc_transcript_variant |
rs12505430 |
Chr4:91584294(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12646630 |
Chr4:21770028(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2172002 |
Chr4:149352962(Fwd) |
intron_variant |
rs12504607 |
Chr4:62513700(Fwd) |
intron_variant; nc_transcript_variant |
rs7672803 |
Chr4:91566875(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs1471221 |
Chr4:21779119(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11730626 |
Chr4:149354289(Fwd) |
intron_variant |
rs6851424 |
Chr4:62513826(Fwd) |
intron_variant; nc_transcript_variant |
rs1040112 |
Chr4:91567664(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs7375384 |
Chr4:21726677(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs10213471 |
Chr4:149370492(Fwd) |
upstream_gene_variant |
rs6551640 |
Chr4:62518821(Fwd) |
intron_variant; nc_transcript_variant |
rs10014992 |
Chr4:91568501(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs1827591 |
Chr4:21732186(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1546043 |
Chr4:149373388(Fwd) |
|
rs4693243 |
Chr4:91568912(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs9994945 |
Chr4:21796843(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6535610 |
Chr4:149377750(Fwd) |
|
rs1841185 |
Chr4:21801107(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1430960 |
Chr4:90553180(Fwd) |
intron_variant; nc_transcript_variant |
rs1490459 |
Chr4:149383136(Fwd) |
|
rs34833395 |
Chr4:21802323(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11933399 |
Chr4:90559006(Fwd) |
intron_variant; nc_transcript_variant |
rs6535612 |
Chr4:149384030(Fwd) |
|
rs1841186 |
Chr4:21804857(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs16996194 |
Chr4:90560529(Fwd) |
intron_variant; nc_transcript_variant |
rs1490462 |
Chr4:149385504(Fwd) |
|
rs4563486 |
Chr4:21809189(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11932021 |
Chr4:90565218(Fwd) |
intron_variant; nc_transcript_variant |
rs2070949 |
Chr4:149358504(Fwd) |
intron_variant; upstream_gene_variant |
rs10938858 |
Chr4:21811875(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11944530 |
Chr4:90565615(Fwd) |
intron_variant; nc_transcript_variant |
rs1565459 |
Chr4:149387520(Fwd) |
|
rs12503736 |
Chr4:21813409(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11933687 |
Chr4:90576512(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4282162 |
Chr4:21817721(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17015956 |
Chr4:90556755(Fwd) |
intron_variant; nc_transcript_variant |
rs1968778 |
Chr4:21818314(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12644119 |
Chr4:90603419(Fwd) |
intron_variant; nc_transcript_variant |
rs4377576 |
Chr4:21825726(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs168625 |
Chr4:21831655(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2007971 |
Chr4:21838132(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2007970 |
Chr4:21838135(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs966045 |
Chr4:21848082(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6840539 |
Chr4:21857733(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs12498561 |
Chr4:21860763(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs7664617 |
Chr4:21862428(Fwd) |
NMD_transcript_variant; intron_variant |
rs1023722 |
Chr4:21057794(Fwd) |
NMD_transcript_variant; intron_variant |
rs10938829 |
Chr4:21094428(Fwd) |
NMD_transcript_variant; intron_variant |
rs12649359 |
Chr4:21115228(Fwd) |
NMD_transcript_variant; intron_variant |
rs16870439 |
Chr4:21138156(Fwd) |
NMD_transcript_variant; intron_variant |
rs16870444 |
Chr4:21144251(Fwd) |
NMD_transcript_variant; intron_variant |
rs16870511 |
Chr4:21170016(Fwd) |
NMD_transcript_variant; intron_variant |
rs4698810 |
Chr4:111019636(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7695878 |
Chr4:21078220(Fwd) |
NMD_transcript_variant; intron_variant |
rs7669237 |
Chr4:111020741(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1865193 |
Chr4:21080564(Fwd) |
NMD_transcript_variant; intron_variant |
rs10032613 |
Chr4:111021758(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6824763 |
Chr4:21089650(Fwd) |
NMD_transcript_variant; intron_variant |
rs3733623 |
Chr4:111026520(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11946639 |
Chr4:21512910(Fwd) |
NMD_transcript_variant; intron_variant |
rs6448011 |
Chr4:21089763(Fwd) |
NMD_transcript_variant; intron_variant |
rs10018930 |
Chr4:111029635(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10018746 |
Chr4:62445246(Fwd) |
intron_variant |
rs358565 |
Chr4:21520182(Fwd) |
NMD_transcript_variant; intron_variant |
rs6448013 |
Chr4:21090037(Fwd) |
NMD_transcript_variant; intron_variant |
rs718815 |
Chr4:111024520(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs35550109 |
Chr4:62462234(Fwd) |
intron_variant; nc_transcript_variant |
rs429783 |
Chr4:21572568(Fwd) |
NMD_transcript_variant; intron_variant |
rs16870359 |
Chr4:21097417(Fwd) |
NMD_transcript_variant; intron_variant |
rs10033229 |
Chr4:111030075(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12642315 |
Chr4:62448934(Fwd) |
intron_variant; upstream_gene_variant |
rs358830 |
Chr4:21588298(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1560789 |
Chr4:21103238(Fwd) |
NMD_transcript_variant; intron_variant |
rs1482469 |
Chr4:111031236(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11131329 |
Chr4:62431199(Fwd) |
intron_variant |
rs1394135 |
Chr4:21598315(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1560788 |
Chr4:21103252(Fwd) |
NMD_transcript_variant; intron_variant |
rs9993301 |
Chr4:62796915(Fwd) |
intron_variant; upstream_gene_variant |
rs1497907 |
Chr4:62433777(Fwd) |
intron_variant |
rs2202312 |
Chr4:21598349(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7696284 |
Chr4:21111675(Fwd) |
NMD_transcript_variant; intron_variant |
rs10026839 |
Chr4:62797061(Fwd) |
intron_variant; upstream_gene_variant |
rs1497906 |
Chr4:62440881(Fwd) |
intron_variant |
rs1394136 |
Chr4:21598374(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7696822 |
Chr4:21111838(Fwd) |
NMD_transcript_variant; intron_variant |
rs10005756 |
Chr4:62800350(Fwd) |
intron_variant; nc_transcript_variant |
rs7669283 |
Chr4:62443715(Fwd) |
intron_variant |
rs10009713 |
Chr4:21600685(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7696531 |
Chr4:21111904(Fwd) |
NMD_transcript_variant; intron_variant |
rs10003942 |
Chr4:62833945(Fwd) |
intron_variant |
rs17239080 |
Chr4:62455462(Fwd) |
intron_variant; nc_transcript_variant |
rs10025434 |
Chr4:21602587(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7696887 |
Chr4:21112046(Fwd) |
NMD_transcript_variant; intron_variant |
rs11131334 |
Chr4:62457454(Fwd) |
intron_variant; nc_transcript_variant |
rs11730697 |
Chr4:21602823(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1897664 |
Chr4:21113049(Fwd) |
NMD_transcript_variant; intron_variant |
rs10866124 |
Chr4:62455858(Fwd) |
intron_variant; nc_transcript_variant |
rs1827593 |
Chr4:21602926(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6448016 |
Chr4:21113124(Fwd) |
NMD_transcript_variant; intron_variant |
rs6551634 |
Chr4:62462328(Fwd) |
intron_variant; nc_transcript_variant |
rs1158161 |
Chr4:21605144(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6814358 |
Chr4:21113282(Fwd) |
NMD_transcript_variant; intron_variant |
rs1021863 |
Chr4:21609078(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1368640 |
Chr4:21114482(Fwd) |
NMD_transcript_variant; intron_variant |
rs6448062 |
Chr4:21614591(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7356370 |
Chr4:21114652(Fwd) |
NMD_transcript_variant; intron_variant |
rs6847761 |
Chr4:21618213(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs11944192 |
Chr4:21114825(Fwd) |
NMD_transcript_variant; intron_variant |
rs6848328 |
Chr4:21618406(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs12643360 |
Chr4:21115056(Fwd) |
NMD_transcript_variant; intron_variant |
rs2340 |
Chr4:21622793(Fwd) |
NMD_transcript_variant; intron_variant |
rs7689193 |
Chr4:21116332(Fwd) |
NMD_transcript_variant; intron_variant |
rs9994077 |
Chr4:21631073(Fwd) |
NMD_transcript_variant; intron_variant |
rs7689340 |
Chr4:21116347(Fwd) |
NMD_transcript_variant; intron_variant |
rs10006027 |
Chr4:21631108(Fwd) |
NMD_transcript_variant; intron_variant |
rs7667541 |
Chr4:21116422(Fwd) |
NMD_transcript_variant; intron_variant |
rs7684408 |
Chr4:75216896(Fwd) |
|
rs16870421 |
Chr4:21116890(Fwd) |
NMD_transcript_variant; intron_variant |
rs7673295 |
Chr4:75217114(Fwd) |
|
rs7673495 |
Chr4:21117046(Fwd) |
NMD_transcript_variant; intron_variant |
rs6446993 |
Chr4:75231866(Fwd) |
intron_variant; nc_transcript_variant |
rs1023721 |
Chr4:21206490(Fwd) |
NMD_transcript_variant; intron_variant |
rs1872455 |
Chr4:21347142(Fwd) |
NMD_transcript_variant; intron_variant |
rs1993665 |
Chr4:75234486(Fwd) |
intron_variant; nc_transcript_variant |
rs12501359 |
Chr4:21361701(Fwd) |
NMD_transcript_variant; intron_variant |
rs1563826 |
Chr4:75235524(Fwd) |
intron_variant; nc_transcript_variant |
rs4235289 |
Chr4:21375088(Fwd) |
NMD_transcript_variant; intron_variant |
rs12512409 |
Chr4:75235789(Fwd) |
intron_variant; nc_transcript_variant |
rs1495523 |
Chr4:21379280(Fwd) |
NMD_transcript_variant; intron_variant |
rs7671661 |
Chr4:75239235(Fwd) |
intron_variant; nc_transcript_variant |
rs17521786 |
Chr4:21380839(Fwd) |
NMD_transcript_variant; intron_variant |
rs2367709 |
Chr4:75248685(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17462325 |
Chr4:21381382(Fwd) |
NMD_transcript_variant; intron_variant |
rs17462464 |
Chr4:21383391(Fwd) |
NMD_transcript_variant; intron_variant |
rs1390261 |
Chr4:21387692(Fwd) |
NMD_transcript_variant; intron_variant |
rs9995524 |
Chr4:21913523(Fwd) |
NMD_transcript_variant; intron_variant |
rs17522576 |
Chr4:21389368(Fwd) |
NMD_transcript_variant; intron_variant |
rs6821401 |
Chr4:21915588(Fwd) |
NMD_transcript_variant; intron_variant |
rs13113329 |
Chr4:21393750(Fwd) |
NMD_transcript_variant; intron_variant |
rs11944614 |
Chr4:21918070(Fwd) |
NMD_transcript_variant; intron_variant |
rs13107161 |
Chr4:21402297(Fwd) |
NMD_transcript_variant; intron_variant |
rs727633 |
Chr4:21920543(Fwd) |
NMD_transcript_variant; intron_variant |
rs1495516 |
Chr4:21404495(Fwd) |
NMD_transcript_variant; intron_variant |
rs10938866 |
Chr4:21922674(Fwd) |
NMD_transcript_variant; intron_variant |
rs1495517 |
Chr4:21404716(Fwd) |
NMD_transcript_variant; intron_variant |
rs1398838 |
Chr4:21916709(Fwd) |
NMD_transcript_variant; intron_variant |
rs1587122 |
Chr4:21411990(Fwd) |
NMD_transcript_variant; intron_variant |
rs10516404 |
Chr4:21918146(Fwd) |
NMD_transcript_variant; intron_variant |
rs6847578 |
Chr4:21412106(Fwd) |
NMD_transcript_variant; intron_variant |
rs9997450 |
Chr4:21919234(Fwd) |
NMD_transcript_variant; intron_variant |
rs12649448 |
Chr4:46744543(Fwd) |
intron_variant |
rs10938868 |
Chr4:21923596(Fwd) |
NMD_transcript_variant; intron_variant |
rs13141126 |
Chr4:46766905(Fwd) |
intron_variant |
rs10938869 |
Chr4:21923741(Fwd) |
NMD_transcript_variant; intron_variant |
rs13119670 |
Chr4:46903491(Fwd) |
intron_variant |
rs12507277 |
Chr4:21925257(Fwd) |
NMD_transcript_variant; intron_variant |
rs16872134 |
Chr4:21927456(Fwd) |
NMD_transcript_variant; intron_variant |
rs10026649 |
Chr4:21928331(Fwd) |
NMD_transcript_variant; intron_variant |
rs10029403 |
Chr4:21929040(Fwd) |
NMD_transcript_variant; intron_variant |
rs13102882 |
Chr4:21931211(Fwd) |
NMD_transcript_variant; intron_variant |
rs13109656 |
Chr4:21931730(Fwd) |
NMD_transcript_variant; intron_variant |
rs10017055 |
Chr4:21932451(Fwd) |
NMD_transcript_variant; intron_variant |
rs13126050 |
Chr4:21934535(Fwd) |
NMD_transcript_variant; intron_variant |
rs12644787 |
Chr4:21972504(Fwd) |
intron_variant; nc_transcript_variant |
rs2007195 |
Chr4:21973217(Fwd) |
intron_variant; nc_transcript_variant |
rs2874977 |
Chr4:21911866(Fwd) |
NMD_transcript_variant; intron_variant |
rs476184 |
Chr4:56246864(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10516405 |
Chr4:21965483(Fwd) |
intron_variant; nc_transcript_variant |
rs483978 |
Chr4:56261089(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10938872 |
Chr4:21969495(Fwd) |
intron_variant; nc_transcript_variant |
rs550144 |
Chr4:56281484(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs1849542 |
Chr4:21973739(Fwd) |
intron_variant; nc_transcript_variant |
rs10462028 |
Chr4:56298300(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs1048004 |
Chr4:56300209(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant |
rs13134269 |
Chr4:129412788(Fwd) |
intron_variant; nc_transcript_variant |
rs17722979 |
Chr4:56346411(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2133430 |
Chr4:129438537(Fwd) |
intron_variant; nc_transcript_variant |
rs2061015 |
Chr4:91849955(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1021307 |
Chr4:56395714(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6821381 |
Chr4:129438919(Fwd) |
intron_variant; nc_transcript_variant |
rs2054334 |
Chr4:91850581(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6851971 |
Chr4:56428064(Fwd) |
intron_variant |
rs6856963 |
Chr4:129444527(Fwd) |
downstream_gene_variant |
rs9307092 |
Chr4:91861595(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs6554290 |
Chr4:56437030(Fwd) |
intron_variant |
rs6856612 |
Chr4:129444528(Fwd) |
downstream_gene_variant |
rs17249857 |
Chr4:91826328(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1037910 |
Chr4:91825652(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6554291 |
Chr4:56437371(Fwd) |
intron_variant |
rs6857394 |
Chr4:129444713(Fwd) |
downstream_gene_variant |
rs11097277 |
Chr4:91828780(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2412664 |
Chr4:56457387(Fwd) |
downstream_gene_variant; intron_variant |
rs7695069 |
Chr4:129445759(Fwd) |
|
rs6532253 |
Chr4:91829559(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs861029 |
Chr4:56245637(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17013394 |
Chr4:129450392(Fwd) |
|
rs7657375 |
Chr4:91833835(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs880358 |
Chr4:56276478(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs13115307 |
Chr4:129403432(Fwd) |
intron_variant; nc_transcript_variant |
rs10012191 |
Chr4:91847796(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17776975 |
Chr4:56276895(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs6824383 |
Chr4:91840449(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs41324951 |
Chr4:56288743(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11097271 |
Chr4:91827917(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6802 |
Chr4:56292101(Fwd) |
3_prime_UTR_variant; downstream_gene_variant |
rs13135875 |
Chr4:91852795(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17721497 |
Chr4:56311248(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs28643477 |
Chr4:91841936(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11240 |
Chr4:56319350(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs7667109 |
Chr4:93463316(Fwd) |
intron_variant; nc_transcript_variant |
rs1993748 |
Chr4:91830699(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2070062 |
Chr4:56355598(Fwd) |
5_prime_UTR_variant; NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant |
rs7700132 |
Chr4:93467282(Fwd) |
intron_variant; nc_transcript_variant |
rs1021306 |
Chr4:56395944(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17019538 |
Chr4:93467552(Fwd) |
intron_variant; nc_transcript_variant |
rs17600510 |
Chr4:168156453(Fwd) |
upstream_gene_variant |
rs7660668 |
Chr4:56401697(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs6532375 |
Chr4:93475443(Fwd) |
intron_variant; nc_transcript_variant |
rs6827192 |
Chr4:168166788(Fwd) |
|
rs7698022 |
Chr4:56407347(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17019568 |
Chr4:93479889(Fwd) |
intron_variant; nc_transcript_variant |
rs6833251 |
Chr4:168166789(Fwd) |
|
rs1979604 |
Chr4:56418755(Fwd) |
downstream_gene_variant |
rs7663643 |
Chr4:93480717(Fwd) |
intron_variant; nc_transcript_variant |
rs10517930 |
Chr4:168180681(Fwd) |
|
rs1979605 |
Chr4:56418873(Fwd) |
downstream_gene_variant |
rs10015220 |
Chr4:6414212(Fwd) |
intron_variant; nc_transcript_variant |
rs1971197 |
Chr4:93452467(Fwd) |
intron_variant; nc_transcript_variant |
rs17600543 |
Chr4:168162185(Fwd) |
|
rs4865012 |
Chr4:56420786(Fwd) |
downstream_gene_variant |
rs9992005 |
Chr4:6414222(Fwd) |
intron_variant; nc_transcript_variant |
rs6848991 |
Chr4:93455252(Fwd) |
intron_variant; nc_transcript_variant |
rs6817102 |
Chr4:168166486(Fwd) |
|
rs6853506 |
Chr4:56424374(Fwd) |
intron_variant |
rs13434456 |
Chr4:6414398(Fwd) |
intron_variant; nc_transcript_variant |
rs7686758 |
Chr4:93463035(Fwd) |
intron_variant; nc_transcript_variant |
rs11933479 |
Chr4:168167952(Fwd) |
|
rs2130040 |
Chr4:56430203(Fwd) |
intron_variant |
rs10213596 |
Chr4:6415208(Fwd) |
intron_variant; nc_transcript_variant |
rs1376115 |
Chr4:93466614(Fwd) |
intron_variant; nc_transcript_variant |
rs13143692 |
Chr4:168168426(Fwd) |
|
rs972446 |
Chr4:56435748(Fwd) |
intron_variant |
rs10213247 |
Chr4:6415329(Fwd) |
intron_variant; nc_transcript_variant |
rs17019530 |
Chr4:93466887(Fwd) |
intron_variant; nc_transcript_variant |
rs10517929 |
Chr4:168168870(Fwd) |
|
rs11732481 |
Chr4:56436379(Fwd) |
intron_variant |
rs10213664 |
Chr4:6415585(Fwd) |
intron_variant; nc_transcript_variant |
rs1376116 |
Chr4:93472319(Fwd) |
intron_variant; nc_transcript_variant |
rs13134784 |
Chr4:168169633(Fwd) |
|
rs10012559 |
Chr4:56437468(Fwd) |
intron_variant |
rs4689000 |
Chr4:6415618(Fwd) |
intron_variant; nc_transcript_variant |
rs7677052 |
Chr4:93475423(Fwd) |
intron_variant; nc_transcript_variant |
rs13113987 |
Chr4:168172399(Fwd) |
|
rs7665846 |
Chr4:56439245(Fwd) |
intron_variant |
rs11724328 |
Chr4:6416437(Fwd) |
intron_variant; nc_transcript_variant |
rs12508375 |
Chr4:93478587(Fwd) |
intron_variant; nc_transcript_variant |
rs17600604 |
Chr4:168174597(Fwd) |
|
rs13133077 |
Chr4:56443809(Fwd) |
intron_variant |
rs11724359 |
Chr4:6416518(Fwd) |
intron_variant; nc_transcript_variant |
rs7699810 |
Chr4:93496946(Fwd) |
intron_variant; nc_transcript_variant |
rs17522294 |
Chr4:168182694(Fwd) |
|
rs2101476 |
Chr4:56445128(Fwd) |
intron_variant |
rs878283 |
Chr4:6421669(Fwd) |
intron_variant; nc_transcript_variant |
rs11730247 |
Chr4:93501374(Fwd) |
intron_variant; nc_transcript_variant |
rs7659452 |
Chr4:168182973(Fwd) |
|
rs4336288 |
Chr4:56450255(Fwd) |
intron_variant |
rs878281 |
Chr4:6422476(Fwd) |
intron_variant; nc_transcript_variant |
rs11934085 |
Chr4:93515166(Fwd) |
intron_variant; nc_transcript_variant |
rs35520897 |
Chr4:168204564(Fwd) |
|
rs6830728 |
Chr4:56451199(Fwd) |
intron_variant |
rs11734695 |
Chr4:6423060(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4404623 |
Chr4:6460154(Fwd) |
intron_variant; nc_transcript_variant |
rs13125393 |
Chr4:168180919(Fwd) |
|