chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733956117733957AG25GENIChomozygous116672236
8117735290117735291TC19GENIChomozygous116672238
8117735631117735632TC40GENIChomozygous116672240
8117736211117736212CT24GENICpossibly homozygous116672242
8117737110117737111GA29GENIChomozygous116672244
8117738201117738202GA31GENIChomozygous116672246
8117738319117738320CA23GENIChomozygous116672248
8117739238117739239TC52GENIChomozygous116672250
8117740083117740084CT28GENICheterozygous116672252
8117740255117740256AG48GENIChomozygous116672254
8117740386117740387AG24GENIChomozygous116672256
8117741469117741470CT19GENIChomozygous116672258
8117742111117742112TG55GENIChomozygous116672262
8117742119117742120TC54GENIChomozygous116672264
8117742500117742501GT28GENIChomozygous116672266
8117742591117742592AG30GENIChomozygous116672270
8117743032117743033AG37GENIChomozygous116672272
8117743124117743125TC37GENIChomozygous116672274
8117744077117744078TA16GENIChomozygous116672276
8117744804117744805TG32GENIChomozygous116672280
8117745435117745436TC39GENIChomozygous116672282
8117746898117746899GT24GENIChomozygous116672284
8117747179117747180AT24GENIChomozygous116672286
8117747861117747862TC27GENIChomozygous116672288
8117752195117752196TC33GENICheterozygous116672290
8117752228117752229CG30GENICheterozygous117005939
8117752230117752231CG30GENICheterozygous117005941
8117752277117752278TG35GENIChomozygous116672292
8117753778117753779GA24GENIChomozygous116672296
8117753889117753890CA25GENIChomozygous116672298
8117772468117772469GT13GENICheterozygous116672300
8117773682117773683GA17GENIChomozygous116672302