chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107505479075054791CA9GENIChomozygous126462247
107505905875059059AG20GENIChomozygous116638109
107506759775067598TC8GENIChomozygous117016766
107506798575067986GA16GENIChomozygous126462248
107506841775068418GA7GENIChomozygous126462249
107507050375070504AT4GENICheterozygous126462250
107507354175073542AG18GENIChomozygous117065454
107507370675073707TC15GENIChomozygous117065456
107507372775073728TC22GENIChomozygous117132018
107507385875073859TC30GENIChomozygous117065458
107507428275074283GA6GENIChomozygous117065460
107507538675075387TC27GENIChomozygous116638119
107507548775075488AG15GENIChomozygous116638121
107507564475075645GA9GENIChomozygous117065462
107507582575075826CG26GENIChomozygous116638123
107507591175075912TC27GENIChomozygous117065464
107507614575076146AT15GENIChomozygous117065466
107507649875076499CT23GENIChomozygous117065468
107507693475076935AG18GENIChomozygous117065470
107507705475077055AG25GENIChomozygous116638127
107507762275077623CT24GENIChomozygous117065472
107507835375078354TC14GENICheterozygous126462251
107507836775078368GA27GENIChomozygous117065474
107507880675078807TC24GENIChomozygous117065476