chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101805285118052852CA21GENIChomozygous68883917
101805686518056866GA15GENIChomozygous68883920
101805646318056464GA27GENIChomozygous68611713
101805777118057772TC20GENIChomozygous67763985
101805790318057904GA19GENIChomozygous68611716
101805820118058202GA15GENICpossibly homozygous68611719
101805867218058673AG16GENIChomozygous67763997
101805944618059447CT19GENIChomozygous68883923
101805950818059509GT17GENIChomozygous68611722
101805955918059560TC12GENIChomozygous67764019
101806000518060006AG16GENIChomozygous68611725
101806223018062231AG20GENIChomozygous68331196