chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4179262980179262981TC27GENIChomozygous952265740
4179287843179287844AT27GENICpossibly homozygous952265741
4179302732179302733TG26GENIChomozygous952265742
4179302733179302734GT28GENIChomozygous952265743
4179315203179315204CT27GENIChomozygous952265744