chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149957363149957364TA11GENIChomozygous112882795
4149958241149958242GA12GENIChomozygous112882796
4149958460149958461GC20GENIChomozygous112882797
4149958581149958582CT25GENIChomozygous112882798
4149959205149959206CT34GENIChomozygous112882799
4149959265149959266TA35GENIChomozygous112882800
4149959266149959267GA36GENIChomozygous112882801
4149959611149959612CA42GENIChomozygous112882802
4149961773149961774AT47GENIChomozygous112882804
4149963628149963629TC33GENIChomozygous112882805
4149963761149963762TC29GENIChomozygous112882806
4149963769149963770AT29GENIChomozygous112882807
4149964471149964472AG36GENIChomozygous112882808
4149965275149965276AG26GENIChomozygous112882809
4149965488149965489TC29GENIChomozygous112882810
4149966429149966430GA33GENIChomozygous112882811
4149969221149969222TC31GENIChomozygous112882812
4149969994149969995GA24GENIChomozygous112882814
4149971468149971469CT41GENIChomozygous112882815
4149973231149973232TG30GENIChomozygous112882816
4149974023149974024TG30GENIChomozygous112882817
4149974054149974055TA22GENIChomozygous112882818
4149974968149974969GA24GENIChomozygous112882819
4149975482149975483GA20GENIChomozygous112882820
4149976181149976182AG10GENIChomozygous112882821
4149976524149976525AG16GENIChomozygous113181654