chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
360713876071387T2GENIChomozygous131837544
360714396071440TC10GENIChomozygous111869087
360724676072468GC42GENICpossibly homozygous111869089
360733916073392CT47GENIChomozygous111869091
360747196074720GA58GENIChomozygous111869093
360783856078386AG65GENICpossibly homozygous111869095