chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403547414035475GC22GENIChomozygous116859636
101403741114037412TG39GENIChomozygous116736601
101403772514037726GC37GENIChomozygous116736602
101403786714037868TC37GENIChomozygous116736603
101403817014038171AG31GENIChomozygous116736604
101403861314038614AG28GENIChomozygous116736605
101403874214038743CT48GENIChomozygous116736606
101403885314038854AG38GENIChomozygous116736607
101403903214039033AC31GENIChomozygous116736608
101404083714040838AG43GENIChomozygous116736609
101404118714041188TC23GENIChomozygous116736610
101404250814042509GA26GENIChomozygous116736611
101404276114042762GA45GENIChomozygous116736612
101404394514043946GA28GENIChomozygous116736613
101404399214043993TG18GENIChomozygous116736614
101404402914044030GC26GENIChomozygous116736616
101404458614044587CT31GENIChomozygous116736617