chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
397928299792830AG47GENIChomozygous111443612
397933039793304TG58GENIChomozygous111443615
397947569794757TC60GENIChomozygous111443621
397953779795378TC56GENIChomozygous111443625
397965629796563TG50GENIChomozygous111443633
397966089796609AG42GENIChomozygous111443634
397967649796764C62GENIChomozygous127848648
397974879797488AG60GENIChomozygous111443639
397936059793606CT54GENIChomozygous111873779
397936419793642CT55GENIChomozygous111873781
397943449794345CT39GENIChomozygous111873783
397941009794103TTA40GENICpossibly homozygous130900450
397978969797897CT48GENICpossibly homozygous111873785
397979039797904CG46GENICpossibly homozygous111873787
397983489798349AC56GENIChomozygous111443641
397986339798634CG57GENIChomozygous111443642
397987149798715AG60GENIChomozygous111443643
397988489798849CT56GENIChomozygous111873789