chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1223118662223118663GA21GENIChomozygous61806269
1223118805223118806TC25GENIChomozygous61806270
1223119081223119082AG25GENIChomozygous61097863
1223119372223119373TTG12GENIChomozygous61806271
1223120010223120011TC29GENIChomozygous61806272
1223120102223120103GA14GENIChomozygous61806273
1223120147223120148TC21GENIChomozygous61097865
1223120163223120164GA22GENIChomozygous61806274
1223120597223120598C-10GENIChomozygous61097866
1223121804223121805GA18GENIChomozygous61806276
1223121864223121873GGGTAGCTA---------17GENIChomozygous61806277
1223123776223123777TG23GENIChomozygous61097869
1223124115223124116AG18GENIChomozygous61097871
1223124371223124372C-11GENIChomozygous61806278
1223124859223124860GA26GENIChomozygous61806279
1223125643223125644TC18GENIChomozygous61097873
1223126165223126166AC17GENIChomozygous61097874
1223126214223126215AG18GENIChomozygous61097875
1223128140223128141CT20GENIChomozygous61806280
1223128520223128521GA24GENIChomozygous61806281
1223130406223130407GC10GENIChomozygous61097881
1223130851223130852TC18GENIChomozygous61097882
1223131822223131823TG16GENIChomozygous61097884
1223131931223131932AG23GENIChomozygous61097885
1223132966223132967AATT8GENICheterozygous61597530
1223132966223132967AAT8GENICheterozygous62102380
1223137194223137195AG17GENIChomozygous61097892
1223138572223138573GGGTTT7GENIChomozygous61097893
1223138679223138680TC12GENIChomozygous61097894
1223140308223140309TTG9GENIChomozygous61806283
1223123777223123778CT24GENIChomozygous62200853