chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1126576920126576921TG67GENIChomozygous778567648
1126577122126577123TC53GENIChomozygous778567649
1126577265126577266CT51GENIChomozygous778567650
1126577324126577325AT69GENICpossibly homozygous778567651
1126577821126577822GT91GENICpossibly homozygous778567652
1126577909126577910TC70GENIChomozygous778567653
1126578055126578056TC62GENIChomozygous778567654
1126578222126578223AG46GENIChomozygous778567655
1126579221126579222CT59GENIChomozygous778567656
1126579396126579397AG56GENIChomozygous778567657
1126579422126579423TC56GENIChomozygous778567658
1126579685126579686TG40GENICpossibly homozygous778567659
1126579696126579697TC46GENICpossibly homozygous778567660
1126581572126581573GA64GENICpossibly homozygous778567661
1126582136126582137CT49GENIChomozygous778567662