chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222893907222893908TC30GENIChomozygous108547565
1222894841222894842TC29GENICpossibly homozygous108547567
1222894868222894869GA24GENIChomozygous108547570
1222896025222896026TC14GENIChomozygous108547572
1222896500222896501CT19GENIChomozygous108547574
1222897443222897444TC18GENIChomozygous108547576
1222899603222899604GA7GENIChomozygous108547578
1222900533222900534AG19GENIChomozygous108547582
1222900886222900887CT21GENIChomozygous108547584
1222901195222901196CA28GENIChomozygous108547586
1222902406222902407TC17GENIChomozygous108547588