chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC18GENIChomozygous117059332
8117733691117733692CT20GENIChomozygous117059334
8117733956117733957AG27GENIChomozygous116672236
8117734405117734406GT22GENIChomozygous117059336
8117734567117734568AG26GENIChomozygous117059338
8117735177117735178AT18GENIChomozygous117059340
8117735437117735438AG20GENIChomozygous117059342
8117735737117735738GT11GENIChomozygous117059344
8117736397117736398CT20GENIChomozygous117059346
8117736417117736418GA19GENIChomozygous117059348
8117736500117736501CT20GENIChomozygous117059350
8117736546117736547AT29GENIChomozygous117059352
8117737230117737231CT17GENIChomozygous117059353
8117738996117738997GA25GENIChomozygous117059355
8117739238117739239TC27GENIChomozygous116672250
8117740471117740472GA22GENIChomozygous117059356
8117740681117740682CT26GENIChomozygous117059357
8117741235117741236GA32GENIChomozygous117059359
8117742119117742120TC20GENIChomozygous116672264
8117742460117742461CT16GENIChomozygous117059360
8117743032117743033AG17GENIChomozygous116672272
8117743124117743125TC21GENIChomozygous116672274
8117743267117743268GA20GENIChomozygous117059362
8117744226117744227AC34GENIChomozygous116672278
8117744439117744440AG15GENIChomozygous117059363
8117744899117744900AG17GENIChomozygous117059365
8117745057117745058GA39GENIChomozygous117059367
8117745414117745415GA36GENIChomozygous117059368
8117745435117745436TC27GENIChomozygous116672282
8117747179117747180AT35GENICpossibly homozygous116672286
8117747496117747497CT39GENIChomozygous117059371
8117747858117747859GA46GENIChomozygous117059375
8117744225117744226TA30GENIChomozygous117912580