chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101805646318056464GA21GENIChomozygous68611713
101805777118057772TC25GENIChomozygous67763985
101805790318057904GA20GENIChomozygous68611716
101805820118058202GA19GENICpossibly homozygous68611719
101805867218058673AG9GENIChomozygous67763997
101805950818059509GT22GENIChomozygous68611722
101805955918059560TC21GENIChomozygous67764019
101806000518060006AG26GENIChomozygous68611725
101806223018062231AG6GENIChomozygous68331196