chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149957363149957364TA4GENIChomozygous112882795
4149958241149958242GA9GENIChomozygous112882796
4149958460149958461GC14GENIChomozygous112882797
4149958581149958582CT12GENIChomozygous112882798
4149959205149959206CT27GENIChomozygous112882799
4149959265149959266TA18GENIChomozygous112882800
4149959266149959267GA18GENIChomozygous112882801
4149959611149959612CA27GENIChomozygous112882802
4149961773149961774AT19GENIChomozygous112882804
4149963628149963629TC38GENIChomozygous112882805
4149963761149963762TC27GENIChomozygous112882806
4149963769149963770AT27GENIChomozygous112882807
4149964471149964472AG37GENIChomozygous112882808
4149965275149965276AG26GENIChomozygous112882809
4149965488149965489TC27GENIChomozygous112882810
4149966429149966430GA32GENIChomozygous112882811
4149969221149969222TC25GENIChomozygous112882812
4149969564149969565TA21GENIChomozygous112882813
4149969994149969995GA21GENIChomozygous112882814
4149971468149971469CT32GENIChomozygous112882815
4149973231149973232TG28GENIChomozygous112882816
4149974023149974024TG20GENIChomozygous112882817
4149974054149974055TA22GENIChomozygous112882818
4149974968149974969GA32GENIChomozygous112882819
4149975482149975483GA25GENIChomozygous112882820
4149976524149976525AG20GENICpossibly homozygous113181654