chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
22624066726240668TA42GENICpossibly homozygous120141144
22624067226240673TC47GENICpossibly homozygous109653556
22624160926241610CT61GENIChomozygous109653560
22624219026242191AG44GENIChomozygous109653565
22624222326242224AG47GENIChomozygous109653567
22624225126242252CG42GENIChomozygous109653569
22624343926243440AG46GENIChomozygous109653571
22624381626243817AG47GENIChomozygous109653573
22624453426244535TC61GENIChomozygous109653575
22624487926244880TC64GENIChomozygous109653579
22624496426244965TC67GENIChomozygous109653581
22624301126243012GA57GENIChomozygous110676099
22624303026243031CT60GENIChomozygous110676101
22624411526244116GA53GENIChomozygous110676103
22624504726245048TC58GENIChomozygous109653583
22624545926245460TC51GENIChomozygous110494366