chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109640662109640663AG15GENIChomozygous116718855
10109641144109641145CT20GENIChomozygous116909631
10109641902109641903CT11GENIChomozygous116909632
10109642568109642569TC15GENIChomozygous116718865
10109643944109643945CT10GENIChomozygous117347095
10109644688109644689CT8GENIChomozygous116909634
10109646395109646396CT14GENIChomozygous116909635
10109650274109650275CT17GENIChomozygous116909636
10109652515109652516TC17GENIChomozygous116718919
10109653806109653807AG17GENIChomozygous116718925
10109654415109654416AG16GENIChomozygous116718935
10109655473109655474GA9GENIChomozygous116909637
10109656144109656145GC13GENIChomozygous118071193