chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99423873494238735TC27GENIChomozygous117390115
99423878194238782TC25GENIChomozygous117390117
99423891794238918GA34GENIChomozygous117390118
99423896394238964AG47GENIChomozygous117390120
99423900194239002CT43GENIChomozygous117390121
99423913494239135GA19GENIChomozygous117601963
99423918894239189TC29GENICpossibly homozygous117390123
99423932694239327GA28GENIChomozygous117390124
99424098994240990CT24GENIChomozygous117390126
99424207294242073GC12GENIChomozygous117390128
99424233294242333AG14GENIChomozygous117390129
99424236494242365AC19GENIChomozygous117390131
99424763094247631AC21GENIChomozygous117390134
99424796994247970AG24GENIChomozygous117390136
99424805794248058AT17GENIChomozygous117601967
99424848494248485CG14GENIChomozygous117601969
99424942394249424TC21GENIChomozygous117390138
99425083194250832CT20GENIChomozygous117390139
99425212494252125AG26GENIChomozygous117390141