chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159318277159318278T11GENIChomozygous127947647
3159318305159318310GTCCC9GENIChomozygous127947648
3159318313159318314G9GENIChomozygous127947649
3159318321159318322GT9GENIChomozygous119915027
3159318325159318325C9GENIChomozygous127947650
3159318333159318333GC8GENIChomozygous127947651
3159318338159318338C8GENIChomozygous127947652
3159318356159318356G8GENIChomozygous127947653
3159318361159318361G8GENIChomozygous127947654
3159318371159318371A7GENIChomozygous127947655
3159318379159318380A4GENIChomozygous127947656
3159318446159318446A8GENIChomozygous130748773
3159318467159318468G6GENIChomozygous130748774
3159318487159318488T5GENIChomozygous130748775
3159318508159318531GAGAGGAGAGAGAAGAGGAGAGA3GENIChomozygous130748776
3159318539159318540A3GENIChomozygous130748777
3159318555159318563AGAGAGAC3GENIChomozygous130748778
3159318577159318607GAGAAAGAGAGAAAGAGAGAAAGAGAGAAG8GENICheterozygous130748779
3159318606159318607G6GENIChomozygous127947657
3159318642159318645CAG8GENIChomozygous127947658
3159318654159318655G8GENIChomozygous127947659
3159318664159318664G8GENIChomozygous127947660
3159318667159318667A8GENIChomozygous127947661
3159318684159318684A8GENIChomozygous127947662
3159318727159318727G13GENIChomozygous127947663
3159318793159318794A20GENIChomozygous127947664
3159318795159318796C20GENIChomozygous127947665
3159318918159318919G22GENIChomozygous127947666
3159318957159318957C24GENIChomozygous127947667
3159318975159318976G21GENIChomozygous127947668
3159319013159319014TC20GENIChomozygous112045325
3159319014159319015GT23GENIChomozygous112045326
3159319017159319018G23GENIChomozygous127947669
3159325938159325938G5GENIChomozygous127947670
3159325940159325941TA5GENIChomozygous111789516
3159318492159318493GC5GENIChomozygous111789512
3159318833159318834GA25GENIChomozygous111789514
3159326014159326015G6GENICheterozygous130748780