chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161324037161324038GT59GENIChomozygous137661486
5161324203161324203GGGGCCTGTCG49GENIChomozygous137351791
5161325053161325053C36GENICpossibly homozygous137351792
5161325080161325081A41GENIChomozygous137351793
5161330091161330092CT53GENIChomozygous137661487
5161331124161331125TG36GENIChomozygous137661488
5161331177161331178AG26GENIChomozygous137661489
5161332235161332236TG50GENIChomozygous137661490
5161332859161332859T59GENIChomozygous137351794
5161334314161334315GC61GENIChomozygous137661491
5161334398161334399AG57GENIChomozygous137661492
5161335104161335105TG43GENIChomozygous137661493
5161335563161335564CT40GENIChomozygous137661494
5161336247161336248AG48GENIChomozygous137661495
5161336252161336253TA46GENIChomozygous137661496