chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173563910735639108CA15GENIChomozygous111034636
173564062435640625GA28GENICpossibly homozygous111034638
173564073735640738GA22GENIChomozygous111034640
173564094335640944TC14GENIChomozygous111034642
173564094835640949AG15GENIChomozygous111034644
173564132535641326CA19GENIChomozygous111034646
173564167435641675GA25GENIChomozygous111034648
173564210535642106TG17GENIChomozygous111034650