chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123882869138828692CT38GENIChomozygous115476469
123882870838828709CT38GENIChomozygous115476471
123882913138829132TC7GENIChomozygous115476475
123882960938829610AG23GENIChomozygous115476477
123883027738830278TC31GENIChomozygous115476479
123883035438830355GA30GENIChomozygous115476481
123883067538830676TC15GENIChomozygous115476483
123883083538830836CT15GENIChomozygous115476485
123883218038832181CT34GENIChomozygous115476487
123883345338833454CT36GENICpossibly homozygous115476489
123883370538833706CT25GENIChomozygous115476491
123883399738833998TC25GENICpossibly homozygous115494020
123883416838834169GA21GENIChomozygous115476493
123883480038834801TC18GENIChomozygous115324098
123883519238835193TC42GENIChomozygous115324100
123883677638836777CA18GENIChomozygous115383075
123883913938839140TA28GENIChomozygous115383077
123883924938839250CT25GENIChomozygous115324122
123883963338839634GA32GENIChomozygous115383079