chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC34GENIChomozygous117059332
8117733691117733692CT56GENIChomozygous117059334
8117733956117733957AG38GENIChomozygous116672236
8117734405117734406GT48GENIChomozygous117059336
8117734567117734568AG71GENIChomozygous117059338
8117735177117735178AT57GENIChomozygous117059340
8117735437117735438AG54GENIChomozygous117059342
8117735737117735738GT36GENIChomozygous117059344
8117736397117736398CT14GENIChomozygous117059346
8117736417117736418GA21GENIChomozygous117059348
8117736500117736501CT63GENIChomozygous117059350
8117736546117736547AT60GENIChomozygous117059352
8117737230117737231CT70GENIChomozygous117059353
8117738996117738997GA50GENIChomozygous117059355
8117739238117739239TC22GENIChomozygous116672250
8117740471117740472GA43GENIChomozygous117059356
8117740681117740682CT53GENIChomozygous117059357
8117741235117741236GA32GENIChomozygous117059359
8117742119117742120TC67GENIChomozygous116672264
8117742460117742461CT29GENICpossibly homozygous117059360
8117743032117743033AG55GENICpossibly homozygous116672272
8117743124117743125TC50GENIChomozygous116672274
8117743267117743268GA56GENIChomozygous117059362
8117744226117744227AC40GENIChomozygous116672278
8117744439117744440AG51GENIChomozygous117059363
8117744804117744805TG42GENIChomozygous116672280
8117744899117744900AG78GENIChomozygous117059365
8117745057117745058GA55GENIChomozygous117059367
8117745414117745415GA37GENIChomozygous117059368
8117745435117745436TC57GENIChomozygous116672282
8117747179117747180AT20GENIChomozygous116672286
8117747496117747497CT48GENIChomozygous117059371
8117747829117747830AG57GENIChomozygous117059373
8117747858117747859GA34GENIChomozygous117059375
8117744225117744226TA39GENIChomozygous117912580