chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3114869511114869512GC39GENIChomozygous112140654
3114872518114872519CT43GENICpossibly homozygous112015262
3114873259114873260GT46GENICheterozygous111680392
3114873287114873288GC22GENIChomozygous111680393
3114873309114873310CA30GENICpossibly homozygous111680394
3114873982114873983CT48GENIChomozygous112140655
3114874574114874575CT41GENICpossibly homozygous112140656
3114877184114877185AG17GENIChomozygous112140657
3114877188114877189AG15GENIChomozygous112140658
3114877192114877193AG17GENIChomozygous112140659
3114877335114877336TC30GENIChomozygous112140660
3114878276114878277TC61GENIChomozygous112015330
3114873261114873262GC43GENICheterozygous112428932
3114873262114873263GT41GENICheterozygous112428933
3114878669114878670AG43GENIChomozygous112015334