chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134769211134769212TC27GENIChomozygous114017277
5134771484134771485AG33GENIChomozygous114017278
5134772262134772263GA34GENIChomozygous114017279
5134773173134773174CT35GENIChomozygous114017280
5134774512134774513GA25GENIChomozygous114017281
5134774940134774941GA25GENIChomozygous114017282
5134775424134775425CT28GENIChomozygous114017283
5134777577134777578GA18GENICheterozygous114340594
5134778993134778994AT24GENIChomozygous114017284
5134780298134780299GA20GENIChomozygous114017285
5134782255134782256AG13GENIChomozygous114017286
5134784510134784511CG46GENIChomozygous114017287
5134784551134784552GA41GENICpossibly homozygous114017288
5134785010134785011GA20GENIChomozygous114017289
5134786315134786316CG21GENIChomozygous114017290
5134787839134787840CT16GENIChomozygous114017291
5134788084134788085GA27GENIChomozygous114017292
5134788311134788312GA12GENIChomozygous114017293
5134789944134789945AG21GENIChomozygous114017294
5134790445134790446GC38GENIChomozygous114017295
5134790665134790666TC25GENIChomozygous114017296
5134792140134792141GA36GENIChomozygous114017297
5134792180134792181GA30GENIChomozygous114017298
5134792214134792215CT25GENIChomozygous114017299
5134792291134792292TG14GENIChomozygous114017300
5134792374134792375AG24GENIChomozygous114017301
5134792549134792550AT25GENIChomozygous114017302
5134792577134792578AT32GENIChomozygous114017303
5134792839134792840TC11GENIChomozygous114017304