chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99423873494238735TC27GENIChomozygous952976886
99423878194238782TC25GENIChomozygous952976887
99423891794238918GA34GENIChomozygous952976888
99423896394238964AG47GENIChomozygous952976889
99423900194239002CT43GENIChomozygous952976890
99423913494239135GA19GENIChomozygous952976891
99423918894239189TC29GENICpossibly homozygous952976892
99423932694239327GA28GENIChomozygous952976893
99424098994240990CT24GENIChomozygous952976894
99424207294242073GC12GENIChomozygous952976895
99424233294242333AG14GENIChomozygous952976896
99424236494242365AC19GENIChomozygous952976897
99424763094247631AC21GENIChomozygous952976898
99424796994247970AG24GENIChomozygous952976899
99424805794248058AT17GENIChomozygous952976900
99424848494248485CG14GENIChomozygous952976901
99424942394249424TC21GENIChomozygous952976902
99425083194250832CT20GENIChomozygous952976903
99425212494252125AG26GENIChomozygous952976904