chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191023003310230034TC16GENIChomozygous140403421
191023045210230453A12GENIChomozygous147376313
191023123510231236TC22GENIChomozygous140403429
191023144810231449AT26GENICpossibly homozygous140403431
191023206710232068GA24GENIChomozygous147377930
191023269010232691TC19GENIChomozygous140403443
191023399010233991TC26GENIChomozygous140403456
191023407610234077AG25GENIChomozygous140403458
191023414110234142TG18GENIChomozygous147377931
191023465010234651GA21GENIChomozygous147377932
191023467110234672AG19GENIChomozygous147377933
191023498210234983CT24GENIChomozygous147377934
191023509510235096TC14GENIChomozygous140403460
191023561610235617TC20GENIChomozygous140403465
191023562410235625TA20GENIChomozygous140403466
191023670410236705CT21GENIChomozygous147377935
191023708610237087TG14GENIChomozygous140403469
191023726010237261GC11GENIChomozygous140403470