chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95268851252688513GT44GENICpossibly homozygous120413089
95269057452690575CT31GENIChomozygous120461030
95269041552690415A20GENICpossibly homozygous131701127
95269061252690613TC41GENIChomozygous117545666
95269182952691830TC49GENIChomozygous117545670
95269416152694162TC55GENICpossibly homozygous117545672
95269425752694258GA38GENIChomozygous117545676
95269517452695175AG56GENIChomozygous117545678
95269676552696766AG50GENIChomozygous117545682
95269767352697674AG41GENIChomozygous117545684
95269902952699030TC55GENIChomozygous117545686
95269908452699085GA56GENIChomozygous120413090
95270136152701362AC38GENIChomozygous117545688
95270173652701737AG50GENIChomozygous117339426
95270230652702307GA62GENIChomozygous117545690
95270302152703022CT35GENIChomozygous117545692
95270464452704645AT56GENIChomozygous120413091
95270700652707007GC59GENIChomozygous117545696
95270763852707639CT59GENIChomozygous117545698
95270845852708459TG61GENIChomozygous117545700
95270913852709138G45GENIChomozygous128711732
95270954552709546GA62GENIChomozygous117545704
95270969952709700A53GENIChomozygous128711733
95271120952711209A43GENICpossibly homozygous128711734
95271165152711652T45GENIChomozygous128711735
95271166652711667GA47GENIChomozygous117545708
95271357452713574G13GENIChomozygous131701128
95271369252713693GA34GENIChomozygous117545712
95271555552715556AG53GENIChomozygous120413093
95271562552715626G61GENIChomozygous128711737
95271562752715628TC62GENIChomozygous117545714
95271602552716026CA42GENIChomozygous117545718
95271609252716093AT51GENIChomozygous117545720
95269729152697292T37GENICheterozygous130773202
95271107152711072GA52GENIChomozygous117528843