chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195601073256010733TC27GENIChomozygous881897226
195601101356011014CT26GENIChomozygous881897227
195601120356011204CT17GENIChomozygous881897228
195601154356011544TC19GENIChomozygous881897229
195601186556011866TG14GENIChomozygous881897230
195601197956011980CT22GENICpossibly homozygous881897231
195601202956012030GA17GENIChomozygous881897232
195601246856012469CA17GENIChomozygous881897233
195601283556012836TC20GENIChomozygous881897234
195601466456014665AG7GENIChomozygous881897235
195601488856014889AT14GENIChomozygous881897236
195601611356016114CA19GENIChomozygous881897237
195601688856016889GA13GENIChomozygous881897238
195601743656017437TA15GENIChomozygous881897239
195601790556017906TC15GENIChomozygous881897240
195601857056018571GA21GENIChomozygous881897241
195601929256019293TC15GENICheterozygous881897242
195601969556019696CT14GENIChomozygous881897243
195601975356019754AG13GENIChomozygous881897244
195601994456019945CT14GENIChomozygous881897245
195602033156020332GA29GENIChomozygous881897246
195602049756020498TC24GENIChomozygous881897247