chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733956117733957AG48GENIChomozygous116672236
8117735290117735291TC56GENIChomozygous116672238
8117735631117735632TC45GENIChomozygous116672240
8117736211117736212CT30GENIChomozygous116672242
8117737110117737111GA41GENICpossibly homozygous116672244
8117738201117738202GA37GENIChomozygous116672246
8117738319117738320CA25GENIChomozygous116672248
8117739238117739239TC46GENIChomozygous116672250
8117740083117740084CT33GENICheterozygous116672252
8117740255117740256AG42GENIChomozygous116672254
8117740386117740387AG47GENIChomozygous116672256
8117741469117741470CT30GENIChomozygous116672258
8117741587117741588GA24GENIChomozygous116672260
8117742111117742112TG45GENIChomozygous116672262
8117742119117742120TC46GENIChomozygous116672264
8117742500117742501GT23GENIChomozygous116672266
8117742512117742513CT22GENIChomozygous116672268
8117742591117742592AG33GENIChomozygous116672270
8117743032117743033AG59GENIChomozygous116672272
8117743124117743125TC56GENIChomozygous116672274
8117744077117744078TA49GENICpossibly homozygous116672276
8117744226117744227AC43GENIChomozygous116672278
8117744804117744805TG42GENIChomozygous116672280
8117745435117745436TC57GENIChomozygous116672282
8117746898117746899GT45GENIChomozygous116672284
8117747179117747180AT47GENIChomozygous116672286
8117747861117747862TC41GENIChomozygous116672288
8117752195117752196TC18GENICheterozygous116672290
8117752277117752278TG33GENIChomozygous116672292
8117753556117753557CA35GENIChomozygous116672294
8117753778117753779GA33GENIChomozygous116672296
8117753889117753890CA23GENICpossibly homozygous116672298
8117772468117772469GT26GENICpossibly homozygous116672300
8117773682117773683GA21GENIChomozygous116672302