chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC23GENIChomozygous117059332
8117733691117733692CT24GENIChomozygous117059334
8117733956117733957AG32GENIChomozygous116672236
8117734405117734406GT37GENICpossibly homozygous117059336
8117734567117734568AG39GENIChomozygous117059338
8117735177117735178AT25GENIChomozygous117059340
8117735437117735438AG20GENIChomozygous117059342
8117735737117735738GT20GENIChomozygous117059344
8117736397117736398CT29GENIChomozygous117059346
8117736417117736418GA32GENIChomozygous117059348
8117736500117736501CT28GENIChomozygous117059350
8117736546117736547AT27GENIChomozygous117059352
8117737230117737231CT16GENIChomozygous117059353
8117738996117738997GA35GENIChomozygous117059355
8117739238117739239TC15GENIChomozygous116672250
8117740471117740472GA33GENIChomozygous117059356
8117740681117740682CT33GENIChomozygous117059357
8117741235117741236GA22GENIChomozygous117059359
8117742119117742120TC27GENIChomozygous116672264
8117742460117742461CT23GENIChomozygous117059360
8117743032117743033AG16GENIChomozygous116672272
8117743124117743125TC12GENIChomozygous116672274
8117743267117743268GA29GENIChomozygous117059362
8117744225117744226TA21GENIChomozygous117912580
8117744226117744227AC22GENIChomozygous116672278
8117744439117744440AG20GENIChomozygous117059363
8117744804117744805TG19GENIChomozygous116672280
8117744899117744900AG29GENIChomozygous117059365
8117745057117745058GA37GENIChomozygous117059367
8117745414117745415GA32GENIChomozygous117059368
8117745435117745436TC33GENIChomozygous116672282
8117747179117747180AT17GENIChomozygous116672286
8117747496117747497CT45GENIChomozygous117059371
8117747829117747830AG35GENIChomozygous117059373
8117747858117747859GA36GENIChomozygous117059375