chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101805646318056464GA50GENIChomozygous68611713
101805777118057772TC39GENIChomozygous67763985
101805790318057904GA30GENIChomozygous68611716
101805820118058202GA24GENICpossibly homozygous68611719
101805867218058673AG35GENICpossibly homozygous67763997
101805950818059509GT38GENIChomozygous68611722
101805955918059560TC29GENIChomozygous67764019
101806000518060006AG47GENIChomozygous68611725
101806223018062231AG37GENIChomozygous68331196