chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4175748501175748503GT17GENICheterozygous130547469
4175769119175769125GGGGGG31GENIChomozygous128107317
4175769129175769129GG34GENIChomozygous128107318
4175769134175769134T35GENIChomozygous128107319
4175769202175769203C46GENIChomozygous128107320
4175769250175769251C42GENIChomozygous128107321
4175769311175769311A41GENIChomozygous128107322
4175769399175769399C34GENIChomozygous128107323
4175769480175769480C20GENIChomozygous128107324
4175769515175769515C26GENIChomozygous128107325
4175769520175769520CC26GENIChomozygous128107326
4175769612175769612G30GENIChomozygous128107327
4175769620175769621G31GENIChomozygous128107328
4175769621175769622AT30GENIChomozygous119283457