chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159318277159318278T36GENIChomozygous127947647
3159318305159318310GTCCC25GENIChomozygous127947648
3159318313159318314G25GENIChomozygous127947649
3159318321159318322GT22GENIChomozygous119915027
3159318325159318325C21GENIChomozygous127947650
3159318333159318333GC15GENIChomozygous127947651
3159318338159318338C15GENIChomozygous127947652
3159318356159318356G13GENIChomozygous127947653
3159318361159318361G12GENIChomozygous127947654
3159318371159318371A12GENIChomozygous127947655
3159318379159318380A8GENIChomozygous127947656
3159318606159318607G3GENIChomozygous127947657
3159318642159318645CAG3GENIChomozygous127947658
3159318654159318655G3GENIChomozygous127947659
3159318664159318664G5GENIChomozygous127947660
3159318667159318667A5GENIChomozygous127947661
3159318684159318684A10GENIChomozygous127947662
3159318727159318727G15GENIChomozygous127947663
3159318793159318794A34GENIChomozygous127947664
3159318795159318796C34GENIChomozygous127947665
3159318833159318834GA38GENIChomozygous111789514
3159318918159318919G48GENIChomozygous127947666
3159318957159318957C41GENIChomozygous127947667
3159318975159318976G47GENIChomozygous127947668
3159319017159319018G43GENIChomozygous127947669
3159319013159319014TC44GENIChomozygous112045325
3159319014159319015GT44GENIChomozygous112045326
3159325938159325938G23GENIChomozygous127947670
3159325940159325941TA22GENIChomozygous111789516