rs_ID |
Location |
Functional Annotation |
rs17462464 |
Chr4:21383391(Fwd) |
NMD_transcript_variant; intron_variant |
rs16872134 |
Chr4:21927456(Fwd) |
NMD_transcript_variant; intron_variant |
rs7688805 |
Chr4:20732334(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17462325 |
Chr4:21381382(Fwd) |
NMD_transcript_variant; intron_variant |
rs10026649 |
Chr4:21928331(Fwd) |
NMD_transcript_variant; intron_variant |
rs17521786 |
Chr4:21380839(Fwd) |
NMD_transcript_variant; intron_variant |
rs10029403 |
Chr4:21929040(Fwd) |
NMD_transcript_variant; intron_variant |
rs1495523 |
Chr4:21379280(Fwd) |
NMD_transcript_variant; intron_variant |
rs13102882 |
Chr4:21931211(Fwd) |
NMD_transcript_variant; intron_variant |
rs4235289 |
Chr4:21375088(Fwd) |
NMD_transcript_variant; intron_variant |
rs9997450 |
Chr4:21919234(Fwd) |
NMD_transcript_variant; intron_variant |
rs9291412 |
Chr4:20727464(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12501359 |
Chr4:21361701(Fwd) |
NMD_transcript_variant; intron_variant |
rs10938868 |
Chr4:21923596(Fwd) |
NMD_transcript_variant; intron_variant |
rs1872455 |
Chr4:21347142(Fwd) |
NMD_transcript_variant; intron_variant |
rs10938869 |
Chr4:21923741(Fwd) |
NMD_transcript_variant; intron_variant |
rs12507277 |
Chr4:21925257(Fwd) |
NMD_transcript_variant; intron_variant |
rs6847578 |
Chr4:21412106(Fwd) |
NMD_transcript_variant; intron_variant |
rs1587122 |
Chr4:21411990(Fwd) |
NMD_transcript_variant; intron_variant |
rs2874977 |
Chr4:21911866(Fwd) |
NMD_transcript_variant; intron_variant |
rs1495517 |
Chr4:21404716(Fwd) |
NMD_transcript_variant; intron_variant |
rs13101486 |
Chr4:21306185(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs1495516 |
Chr4:21404495(Fwd) |
NMD_transcript_variant; intron_variant |
rs983071 |
Chr4:21306814(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs13107161 |
Chr4:21402297(Fwd) |
NMD_transcript_variant; intron_variant |
rs13109656 |
Chr4:21931730(Fwd) |
NMD_transcript_variant; intron_variant |
rs13108702 |
Chr4:21307087(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs13113329 |
Chr4:21393750(Fwd) |
NMD_transcript_variant; intron_variant |
rs10017055 |
Chr4:21932451(Fwd) |
NMD_transcript_variant; intron_variant |
rs13120431 |
Chr4:21312027(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17522576 |
Chr4:21389368(Fwd) |
NMD_transcript_variant; intron_variant |
rs13126050 |
Chr4:21934535(Fwd) |
NMD_transcript_variant; intron_variant |
rs12643751 |
Chr4:21316608(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1390261 |
Chr4:21387692(Fwd) |
NMD_transcript_variant; intron_variant |
rs2007762 |
Chr4:21301546(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs10938866 |
Chr4:21922674(Fwd) |
NMD_transcript_variant; intron_variant |
rs727633 |
Chr4:21920543(Fwd) |
NMD_transcript_variant; intron_variant |
rs10516404 |
Chr4:21918146(Fwd) |
NMD_transcript_variant; intron_variant |
rs1398838 |
Chr4:21916709(Fwd) |
NMD_transcript_variant; intron_variant |
rs9995524 |
Chr4:21913523(Fwd) |
NMD_transcript_variant; intron_variant |
rs11944614 |
Chr4:21918070(Fwd) |
NMD_transcript_variant; intron_variant |
rs6821401 |
Chr4:21915588(Fwd) |
NMD_transcript_variant; intron_variant |
rs10006027 |
Chr4:21631108(Fwd) |
NMD_transcript_variant; intron_variant |
rs9994077 |
Chr4:21631073(Fwd) |
NMD_transcript_variant; intron_variant |
rs2340 |
Chr4:21622793(Fwd) |
NMD_transcript_variant; intron_variant |
rs6848328 |
Chr4:21618406(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs6847761 |
Chr4:21618213(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs6448062 |
Chr4:21614591(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1021863 |
Chr4:21609078(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1158161 |
Chr4:21605144(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1827593 |
Chr4:21602926(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11730697 |
Chr4:21602823(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10025434 |
Chr4:21602587(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10009713 |
Chr4:21600685(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1394136 |
Chr4:21598374(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2202312 |
Chr4:21598349(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs358830 |
Chr4:21588298(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1394135 |
Chr4:21598315(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs358565 |
Chr4:21520182(Fwd) |
NMD_transcript_variant; intron_variant |
rs429783 |
Chr4:21572568(Fwd) |
NMD_transcript_variant; intron_variant |
rs11946639 |
Chr4:21512910(Fwd) |
NMD_transcript_variant; intron_variant |
rs7664617 |
Chr4:21862428(Fwd) |
NMD_transcript_variant; intron_variant |
rs4563486 |
Chr4:21809189(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10938858 |
Chr4:21811875(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12503736 |
Chr4:21813409(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4282162 |
Chr4:21817721(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs9994945 |
Chr4:21796843(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1841185 |
Chr4:21801107(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs34833395 |
Chr4:21802323(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1841186 |
Chr4:21804857(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 |
rs1968778 |
Chr4:21818314(Fwd) |
NMD_transcript_variant; 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 |
rs10031539 |
Chr4:21759229(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1380270 |
Chr4:21755399(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17498679 |
Chr4:21761746(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6856781 |
Chr4:21759766(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs6448075 |
Chr4:21752712(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4696975 |
Chr4:21318171(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs9291430 |
Chr4:21745448(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs13118906 |
Chr4:21317300(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2018175 |
Chr4:21754408(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs13108412 |
Chr4:21314195(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1459274 |
Chr4:21753319(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11734360 |
Chr4:21310634(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1471221 |
Chr4:21779119(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12646630 |
Chr4:21770028(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1827591 |
Chr4:21732186(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7375384 |
Chr4:21726677(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs1809267 |
Chr4:21768895(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17498715 |
Chr4:21762186(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs35609084 |
Chr4:21769939(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1562815 |
Chr4:21769253(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs16870439 |
Chr4:21138156(Fwd) |
NMD_transcript_variant; intron_variant |
rs10034603 |
Chr4:21729953(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs12649359 |
Chr4:21115228(Fwd) |
NMD_transcript_variant; intron_variant |
rs9884923 |
Chr4:21719296(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs16870511 |
Chr4:21170016(Fwd) |
NMD_transcript_variant; intron_variant |
rs16870444 |
Chr4:21144251(Fwd) |
NMD_transcript_variant; intron_variant |
rs6448072 |
Chr4:21743231(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7378252 |
Chr4:21734789(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10938829 |
Chr4:21094428(Fwd) |
NMD_transcript_variant; intron_variant |
rs6448069 |
Chr4:21734198(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1023722 |
Chr4:21057794(Fwd) |
NMD_transcript_variant; intron_variant |
rs10012747 |
Chr4:21730447(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs16870359 |
Chr4:21097417(Fwd) |
NMD_transcript_variant; intron_variant |
rs6448013 |
Chr4:21090037(Fwd) |
NMD_transcript_variant; intron_variant |
rs1560788 |
Chr4:21103252(Fwd) |
NMD_transcript_variant; intron_variant |
rs1560789 |
Chr4:21103238(Fwd) |
NMD_transcript_variant; intron_variant |
rs1865193 |
Chr4:21080564(Fwd) |
NMD_transcript_variant; intron_variant |
rs7695878 |
Chr4:21078220(Fwd) |
NMD_transcript_variant; intron_variant |
rs6448011 |
Chr4:21089763(Fwd) |
NMD_transcript_variant; intron_variant |
rs6824763 |
Chr4:21089650(Fwd) |
NMD_transcript_variant; intron_variant |
rs1897664 |
Chr4:21113049(Fwd) |
NMD_transcript_variant; intron_variant |
rs6448016 |
Chr4:21113124(Fwd) |
NMD_transcript_variant; intron_variant |
rs6814358 |
Chr4:21113282(Fwd) |
NMD_transcript_variant; intron_variant |
rs1368640 |
Chr4:21114482(Fwd) |
NMD_transcript_variant; intron_variant |
rs7696284 |
Chr4:21111675(Fwd) |
NMD_transcript_variant; intron_variant |
rs7696822 |
Chr4:21111838(Fwd) |
NMD_transcript_variant; intron_variant |
rs7696531 |
Chr4:21111904(Fwd) |
NMD_transcript_variant; intron_variant |
rs7696887 |
Chr4:21112046(Fwd) |
NMD_transcript_variant; intron_variant |
rs7689340 |
Chr4:21116347(Fwd) |
NMD_transcript_variant; intron_variant |
rs7667541 |
Chr4:21116422(Fwd) |
NMD_transcript_variant; intron_variant |
rs16870421 |
Chr4:21116890(Fwd) |
NMD_transcript_variant; intron_variant |
rs7673495 |
Chr4:21117046(Fwd) |
NMD_transcript_variant; intron_variant |
rs7356370 |
Chr4:21114652(Fwd) |
NMD_transcript_variant; intron_variant |
rs11944192 |
Chr4:21114825(Fwd) |
NMD_transcript_variant; intron_variant |
rs12643360 |
Chr4:21115056(Fwd) |
NMD_transcript_variant; intron_variant |
rs7689193 |
Chr4:21116332(Fwd) |
NMD_transcript_variant; intron_variant |
rs9291413 |
Chr4:20861032(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1388321 |
Chr4:20880744(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1844812 |
Chr4:20856032(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10938814 |
Chr4:20856297(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10938815 |
Chr4:20856353(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12505671 |
Chr4:20857040(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2874862 |
Chr4:20853751(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7669354 |
Chr4:20854588(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7669387 |
Chr4:20854640(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs3765120 |
Chr4:20852001(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs3765121 |
Chr4:20852166(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant; splice_region_variant; synonymous_variant |
rs3765122 |
Chr4:20852244(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
rs10938811 |
Chr4:20853065(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7673250 |
Chr4:20850986(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7694587 |
Chr4:20850880(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs3765119 |
Chr4:20851969(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs4697193 |
Chr4:20851191(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1158971 |
Chr4:20866586(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12645522 |
Chr4:20856831(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1023721 |
Chr4:21206490(Fwd) |
NMD_transcript_variant; intron_variant |