chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159318277159318278T13GENIChomozygous127947647
3159318305159318310GTCCC11GENIChomozygous127947648
3159318313159318314G11GENIChomozygous127947649
3159318321159318322GT11GENIChomozygous119915027
3159318325159318325C11GENIChomozygous127947650
3159318333159318333GC8GENIChomozygous127947651
3159318338159318338C6GENIChomozygous127947652
3159318356159318356G5GENIChomozygous127947653
3159318361159318361G4GENIChomozygous127947654
3159318371159318371A3GENIChomozygous127947655
3159318379159318380A3GENIChomozygous127947656
3159318642159318645CAG4GENIChomozygous127947658
3159318654159318655G5GENIChomozygous127947659
3159318664159318664G6GENIChomozygous127947660
3159318667159318667A7GENIChomozygous127947661
3159318684159318684A10GENIChomozygous127947662
3159318727159318727G14GENIChomozygous127947663
3159318793159318794A20GENIChomozygous127947664
3159318795159318796C20GENIChomozygous127947665
3159318918159318919G22GENIChomozygous127947666
3159318957159318957C17GENIChomozygous127947667
3159318975159318976G16GENIChomozygous127947668
3159319017159319018G20GENIChomozygous127947669
3159318833159318834GA19GENIChomozygous111789514
3159319013159319014TC21GENIChomozygous112045325
3159319014159319015GT20GENIChomozygous112045326
3159325938159325938G7GENIChomozygous127947670
3159325940159325941TA7GENIChomozygous111789516