chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149957363149957364TA42GENIChomozygous112882795
4149958241149958242GA49GENIChomozygous112882796
4149958460149958461GC39GENIChomozygous112882797
4149958581149958582CT55GENIChomozygous112882798
4149959205149959206CT55GENIChomozygous112882799
4149959265149959266TA68GENIChomozygous112882800
4149959266149959267GA68GENIChomozygous112882801
4149959611149959612CA53GENIChomozygous112882802
4149961267149961268GA16GENICheterozygous112882803
4149961773149961774AT67GENIChomozygous112882804
4149963628149963629TC61GENIChomozygous112882805
4149963761149963762TC92GENICpossibly homozygous112882806
4149963769149963770AT82GENIChomozygous112882807
4149964471149964472AG64GENIChomozygous112882808
4149965275149965276AG36GENIChomozygous112882809
4149965488149965489TC76GENIChomozygous112882810
4149966429149966430GA51GENIChomozygous112882811
4149969221149969222TC81GENIChomozygous112882812
4149969564149969565TA64GENIChomozygous112882813
4149969994149969995GA58GENIChomozygous112882814
4149971468149971469CT65GENIChomozygous112882815
4149973231149973232TG70GENIChomozygous112882816
4149976181149976182AG40GENICpossibly homozygous112882821
4149974023149974024TG81GENIChomozygous112882817
4149974054149974055TA88GENIChomozygous112882818
4149974968149974969GA62GENIChomozygous112882819
4149975482149975483GA80GENIChomozygous112882820