chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC30GENIChomozygous117059332
8117733691117733692CT28GENIChomozygous117059334
8117733956117733957AG23GENIChomozygous116672236
8117734405117734406GT29GENIChomozygous117059336
8117734567117734568AG28GENIChomozygous117059338
8117735177117735178AT12GENIChomozygous117059340
8117735437117735438AG23GENIChomozygous117059342
8117735737117735738GT11GENIChomozygous117059344
8117736397117736398CT15GENIChomozygous117059346
8117736417117736418GA19GENIChomozygous117059348
8117736500117736501CT17GENIChomozygous117059350
8117736546117736547AT19GENIChomozygous117059352
8117737230117737231CT18GENIChomozygous117059353
8117738996117738997GA35GENIChomozygous117059355
8117739238117739239TC20GENIChomozygous116672250
8117740386117740387AG14GENIChomozygous116672256
8117740471117740472GA29GENIChomozygous117059356
8117740681117740682CT22GENIChomozygous117059357
8117741235117741236GA36GENIChomozygous117059359
8117742119117742120TC29GENIChomozygous116672264
8117742460117742461CT18GENIChomozygous117059360
8117743032117743033AG28GENIChomozygous116672272
8117743267117743268GA26GENIChomozygous117059362
8117744226117744227AC22GENIChomozygous116672278
8117744439117744440AG18GENIChomozygous117059363
8117744804117744805TG22GENIChomozygous116672280
8117745057117745058GA39GENIChomozygous117059367
8117745414117745415GA35GENIChomozygous117059368
8117745435117745436TC29GENIChomozygous116672282
8117747179117747180AT20GENIChomozygous116672286
8117747496117747497CT38GENIChomozygous117059371
8117747829117747830AG28GENICpossibly homozygous117059373
8117747858117747859GA25GENIChomozygous117059375
8117744225117744226TA21GENIChomozygous117912580