chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733956117733957AG24GENIChomozygous116672236
8117735290117735291TC23GENIChomozygous116672238
8117735631117735632TC17GENIChomozygous116672240
8117736211117736212CT15GENICpossibly homozygous116672242
8117737110117737111GA15GENIChomozygous116672244
8117738201117738202GA29GENIChomozygous116672246
8117738319117738320CA21GENIChomozygous116672248
8117739238117739239TC24GENIChomozygous116672250
8117740083117740084CT26GENICheterozygous116672252
8117740255117740256AG23GENICpossibly homozygous116672254
8117740386117740387AG26GENIChomozygous116672256
8117741469117741470CT13GENIChomozygous116672258
8117741587117741588GA16GENIChomozygous116672260
8117742111117742112TG27GENIChomozygous116672262
8117742119117742120TC28GENIChomozygous116672264
8117742500117742501GT19GENICpossibly homozygous116672266
8117742591117742592AG23GENIChomozygous116672270
8117743032117743033AG16GENIChomozygous116672272
8117743124117743125TC18GENIChomozygous116672274
8117744077117744078TA23GENIChomozygous116672276
8117744804117744805TG26GENIChomozygous116672280
8117745435117745436TC24GENIChomozygous116672282
8117746898117746899GT19GENIChomozygous116672284
8117747179117747180AT26GENIChomozygous116672286
8117747861117747862TC21GENIChomozygous116672288
8117752195117752196TC12GENICheterozygous116672290
8117752277117752278TG21GENIChomozygous116672292
8117752526117752527AG17GENIChomozygous116988183
8117753556117753557CA14GENIChomozygous116672294
8117753778117753779GA11GENIChomozygous116672296
8117753889117753890CA10GENIChomozygous116672298