chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4167943658167943659GC36GENIChomozygous144687472
4167944447167944447A57GENICpossibly homozygous144661540
4167944596167944597GA53GENIChomozygous144687473
4167944695167944696TC64GENIChomozygous144687474
4167944706167944707TC56GENIChomozygous144687475
4167946110167946111GA36GENIChomozygous144687476
4167946145167946146CT29GENIChomozygous144687477
4167947439167947440GA48GENIChomozygous144687478
4167947716167947716AT43GENIChomozygous144661541
4167947892167947892T28GENICpossibly homozygous144661542
4167948019167948020TG40GENIChomozygous144687479
4167948052167948053GC38GENIChomozygous144687480
4167948434167948434A35GENIChomozygous144661543
4167951064167951065AG30GENIChomozygous144687481
4167951333167951342CACCACCAC42GENIChomozygous144661544
4167951360167951375CACCACCATCACCAC41GENIChomozygous144661545
4167951613167951614GA47GENIChomozygous144687482
4167951860167951861AG47GENIChomozygous144687483
4167952499167952500CT41GENIChomozygous144687484
4167952594167952595TC37GENIChomozygous144687485
4167952728167952729GC37GENIChomozygous144687486
4167952746167952746T39GENIChomozygous136928332
4167953096167953097GA44GENIChomozygous144687487
4167953284167953285CT55GENIChomozygous144687488
4167953311167953312GA59GENIChomozygous144687489
4167954291167954292CT40GENIChomozygous137263071
4167952544167952545TC44GENIChomozygous137263070
4167955207167955208TC52GENIChomozygous137263072