chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X6889190968891910AC11GENIChomozygous971480534
X6889198568891986GA7GENIChomozygous971480535
X6889235368892354CT18GENIChomozygous971480536
X6889294168892942CT12GENICpossibly homozygous971480537
X6889339968893400CT12GENIChomozygous971480538
X6889355068893551TC14GENIChomozygous971480539
X6889478168894782CG16GENIChomozygous971480540
X6889712168897122GA17GENIChomozygous971480541
X6889869768898698AC15GENIChomozygous971480542
X6889942168899422TC12GENIChomozygous971480543