chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99423873494238735TC21GENIChomozygous955698646
99423878194238782TC25GENIChomozygous955698647
99423891794238918GA25GENIChomozygous955698648
99423896394238964AG33GENIChomozygous955698649
99423900194239002CT37GENIChomozygous955698650
99423913494239135GA49GENIChomozygous955698651
99423918894239189TC42GENIChomozygous955698652
99423932694239327GA34GENIChomozygous955698653
99424098994240990CT25GENIChomozygous955698654
99424207294242073GC24GENIChomozygous955698655
99424233294242333AG33GENIChomozygous955698656
99424236494242365AC29GENIChomozygous955698657
99424750794247508GA23GENIChomozygous955698658
99424763094247631AC28GENIChomozygous955698659
99424796994247970AG40GENIChomozygous955698660
99424805794248058AT29GENIChomozygous955698661
99424848494248485CG28GENIChomozygous955698662
99424942394249424TC27GENIChomozygous955698663
99425083194250832CT26GENICpossibly homozygous955698664
99425212494252125AG31GENIChomozygous955698665