chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105695458956954590TC52GENIChomozygous116603097
105695691056956911CT40GENIChomozygous117060024
105695930756959308GA59GENICpossibly homozygous116603105
105695940056959401GC58GENICpossibly homozygous116603107
105695949056959491AG57GENIChomozygous116935953
105696173056961731AG46GENICpossibly homozygous116935955
105696099756960998G49GENICpossibly homozygous131094660
105696012756960128G44GENIChomozygous131094659