chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8113222360113222361AG14GENIChomozygous184732880
8113222501113222502CT4GENIChomozygous184732881
8113222503113222504CT3GENIChomozygous184732882
8113224278113224279TC19GENIChomozygous186827327
8113224315113224316AG23GENICpossibly homozygous186827328
8113225770113225771AT3GENIChomozygous186827329
8113225890113225891CT4GENIChomozygous186827330
8113226964113226965AG13GENIChomozygous186827331
8113227137113227138GA17GENIChomozygous186827332
8113227609113227610TC19GENIChomozygous184732883
8113227719113227720TG11GENIChomozygous184732884
8113228003113228004CT25GENIChomozygous186827333
8113228797113228798GA18GENIChomozygous186827334
8113230415113230416AG23GENIChomozygous184732885
8113230836113230837CT20GENIChomozygous186827335
8113231473113231474GA21GENIChomozygous184732886
8113232169113232170TC16GENIChomozygous186827336
8113232542113232543TC17GENIChomozygous186827337
8113232675113232676GA20GENIChomozygous186827338
8113232745113232746TC22GENIChomozygous186827339
8113232924113232925CT22GENIChomozygous184732887
8113233672113233673CT14GENIChomozygous186827340
8113233767113233768GA17GENIChomozygous186827341
8113233985113233986TC11GENIChomozygous186827342
8113234949113234950CT18GENIChomozygous184732888
8113235068113235069AT17GENIChomozygous184732889
8113235563113235564AG21GENIChomozygous184732890
8113235612113235613GA15GENIChomozygous184732891
8113236137113236138CT18GENIChomozygous186827343
8113236564113236565GA19GENIChomozygous184732892
8113236870113236871CT19GENIChomozygous184732893
8113237068113237069GA22GENIChomozygous184732894
8113237988113237989GA18GENICpossibly homozygous184732895
8113238400113238401GA25GENIChomozygous186827344
8113238626113238627GA28GENIChomozygous186827345
8113239755113239756CT18GENIChomozygous184732896
8113240097113240098AG32GENIChomozygous186827346
8113240441113240442AT15GENIChomozygous184732897