chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC34GENIChomozygous117059332
8117733691117733692CT34GENIChomozygous117059334
8117733956117733957AG29GENIChomozygous116672236
8117734405117734406GT36GENIChomozygous117059336
8117734567117734568AG35GENIChomozygous117059338
8117735177117735178AT44GENIChomozygous117059340
8117735437117735438AG36GENIChomozygous117059342
8117735737117735738GT38GENIChomozygous117059344
8117736397117736398CT33GENIChomozygous117059346
8117736417117736418GA39GENIChomozygous117059348
8117736500117736501CT35GENIChomozygous117059350
8117736546117736547AT36GENIChomozygous117059352
8117737230117737231CT45GENICpossibly homozygous117059353
8117738996117738997GA30GENIChomozygous117059355
8117739238117739239TC33GENIChomozygous116672250
8117740386117740387AG33GENIChomozygous116672256
8117740471117740472GA27GENIChomozygous117059356
8117740681117740682CT41GENIChomozygous117059357
8117741235117741236GA40GENIChomozygous117059359
8117742119117742120TC53GENIChomozygous116672264
8117742460117742461CT36GENIChomozygous117059360
8117743032117743033AG36GENIChomozygous116672272
8117743124117743125TC47GENIChomozygous116672274
8117743267117743268GA50GENIChomozygous117059362
8117744439117744440AG47GENIChomozygous117059363
8117744804117744805TG32GENIChomozygous116672280
8117744899117744900AG46GENIChomozygous117059365
8117745057117745058GA47GENIChomozygous117059367
8117745414117745415GA31GENIChomozygous117059368
8117745435117745436TC31GENIChomozygous116672282
8117745965117745966GA34GENICheterozygous117059370
8117747179117747180AT34GENIChomozygous116672286
8117747496117747497CT36GENIChomozygous117059371
8117747829117747830AG38GENIChomozygous117059373
8117747858117747859GA38GENIChomozygous117059375
8117773682117773683GA24GENIChomozygous116672302
8117772546117772547GC17GENIChomozygous117125107
8117769392117769393CT28GENICheterozygous117125105