chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123830872838308729TC25GENIChomozygous790919266
123830885538308856TC20GENIChomozygous790919267
123830898638308987CT28GENIChomozygous790919268
123831211138312112CT150GENICheterozygous790919269
123831212638312127CT157GENICheterozygous790919270
123831212738312128AG155GENICheterozygous790919271
123831213438312135CT173GENICheterozygous790919272
123831852838318529GT17GENICpossibly homozygous790919273
123832602338326024TA21GENIChomozygous790919274
123832603738326038AG23GENIChomozygous790919275
123832655038326551GA28GENIChomozygous790919276
123832661038326611AG23GENIChomozygous790919277
123832666038326661TG37GENIChomozygous790919278
123832668738326688CT35GENIChomozygous790919279