chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122539944122539945CT17GENIChomozygous115860892
7122540053122540054TC21GENIChomozygous115860894
7122542658122542659GA19GENIChomozygous115860896
7122543559122543560CA9GENIChomozygous115860898
7122545534122545535AG25GENIChomozygous115860900
7122548356122548357AT20GENIChomozygous115860902
7122548718122548719CA14GENIChomozygous115860904
7122550881122550882AG22GENIChomozygous115860906
7122551704122551705CT21GENIChomozygous115860908
7122560055122560056TC20GENIChomozygous115860920
7122563717122563718GA19GENIChomozygous115860922
7122565436122565437CG24GENIChomozygous115860924
7122566081122566082CT13GENIChomozygous115860926
7122567026122567027GA17GENIChomozygous115860928
7122552135122552135G5GENIChomozygous128513472
7122552152122552153G4GENIChomozygous128513473
7122559376122559376T20GENIChomozygous128513475
7122563635122563636A18GENIChomozygous128513476
7122568574122568575TA15GENIChomozygous115860930
7122569085122569086G15GENIChomozygous128513479
7122573650122573651AG17GENIChomozygous115860933
7122574735122574736AG18GENIChomozygous115860935
7122574753122574754TA19GENIChomozygous115860937
7122574999122574999CTC26GENIChomozygous128513480
7122577597122577598AG14GENIChomozygous115860941
7122578861122578861TGGTGATGGTGTTGTTGG7GENIChomozygous128513481
7122578961122578963TC4GENIChomozygous128513486
7122578966122578966G5GENIChomozygous128513487
7122578975122578975A7GENIChomozygous128513488
7122578981122578981A8GENIChomozygous128513489
7122578986122578986G8GENIChomozygous128513490
7122578994122578995A11GENIChomozygous128513491
7122579026122579027T13GENIChomozygous128513492
7122579037122579038A14GENIChomozygous128513493
7122579044122579044CC14GENIChomozygous128513494
7122579456122579457AG18GENIChomozygous115860943
7122580221122580222AG28GENIChomozygous115860945
7122581613122581614GA14GENIChomozygous115860947
7122581619122581620AG14GENIChomozygous115860949