chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8122531781122531782TC47GENIChomozygous116690950
8122532480122532487TTTTTTG6GENICheterozygous130673029
8122532530122532531C6GENIChomozygous128640471
8122532554122532556CG11GENIChomozygous128640472
8122532560122532562GT11GENIChomozygous128640473
8122532564122532564T11GENIChomozygous128640474
8122532574122532575C10GENIChomozygous128640475
8122532590122532592TA11GENIChomozygous128640476
8122532635122532636G14GENIChomozygous128640477
8122532640122532641T14GENIChomozygous128640478
8122532665122532666T15GENIChomozygous128640479
8122532685122532686G17GENIChomozygous128640480
8122532722122532723CG1GENIChomozygous116690952
8122532730122532731T1GENIChomozygous128640481
8122532770122532771T2GENIChomozygous128640482
8122532781122532782TC3GENIChomozygous116690954
8122533028122533029TC15GENIChomozygous116690956
8122533204122533205GC33GENIChomozygous116690958
8122534416122534417AG33GENIChomozygous116690960
8122534420122534421CT32GENIChomozygous116690962
8122534699122534699C34GENICpossibly homozygous128640483
8122534906122534906AC13GENIChomozygous128640484
8122535467122535468AG26GENIChomozygous126706546
8122532666122532667TG15GENIChomozygous117969432