chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8122531781122531782TC27GENIChomozygous116690950
8122532480122532487TTTTTTG7GENICheterozygous130673029
8122532564122532564T13GENIChomozygous128640474
8122532530122532531C6GENIChomozygous128640471
8122532554122532556CG11GENIChomozygous128640472
8122532560122532562GT12GENIChomozygous128640473
8122532574122532575C13GENIChomozygous128640475
8122532590122532592TA16GENIChomozygous128640476
8122532635122532636G21GENIChomozygous128640477
8122532640122532641T20GENIChomozygous128640478
8122532665122532666T20GENIChomozygous128640479
8122532685122532686G21GENIChomozygous128640480
8122532722122532723CG14GENIChomozygous116690952
8122532730122532731T14GENIChomozygous128640481
8122532770122532771T8GENIChomozygous128640482
8122532781122532782TC10GENIChomozygous116690954
8122533028122533029TC10GENIChomozygous116690956
8122533204122533205GC33GENIChomozygous116690958
8122534416122534417AG43GENIChomozygous116690960
8122534420122534421CT40GENIChomozygous116690962
8122534699122534699C32GENICheterozygous128640483
8122535467122535468AG23GENIChomozygous126706546
8122532666122532667TG20GENIChomozygous117969432
8122534906122534906AC45GENIChomozygous128640484