chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89974038799740388TC15GENICpossibly homozygous116600652
89974047199740472GA21GENIChomozygous116600654
89974073399740734CG18GENIChomozygous116600656
89974150299741503CA18GENICheterozygous116600658
89974289599742896AG30GENICpossibly homozygous116600660
89974289899742899AG30GENIChomozygous116600662
89974290299742903TC30GENIChomozygous116600664
89974291299742913GA34GENIChomozygous116600666
89974295899742959GA32GENIChomozygous116600668
89974392999743930CT26GENICpossibly homozygous116600670
89974404399744044CG23GENIChomozygous116600672
89974406899744069AC19GENIChomozygous116600674
89977476099774761GA10GENIChomozygous116600676
89977598999775990CT29GENIChomozygous116600678
89977622599776226CT17GENIChomozygous116600680
89977709399777094AT23GENIChomozygous116600682
89977950799779508CT19GENIChomozygous116600684
89977985799779858AG21GENIChomozygous116600686
89978105899781059AG17GENIChomozygous116600688
89978136599781366TC21GENIChomozygous116600690
89978173799781738TA15GENIChomozygous116600692
89978185099781851TG9GENIChomozygous116600694