chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161324037161324038GT13GENIChomozygous137661486
5161324203161324203GGGGCCTGTCG17GENIChomozygous137351791
5161325053161325053C14GENIChomozygous137351792
5161325080161325081A15GENICpossibly homozygous137351793
5161330091161330092CT8GENIChomozygous137661487
5161331124161331125TG11GENIChomozygous137661488
5161331177161331178AG6GENIChomozygous137661489
5161332235161332236TG15GENIChomozygous137661490
5161332859161332859T14GENIChomozygous137351794
5161334314161334315GC24GENIChomozygous137661491
5161334398161334399AG20GENIChomozygous137661492
5161335104161335105TG23GENIChomozygous137661493
5161335563161335564CT16GENIChomozygous137661494
5161336247161336248AG16GENIChomozygous137661495
5161336252161336253TA15GENIChomozygous137661496