chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC11GENIChomozygous117059332
8117733691117733692CT7GENIChomozygous117059334
8117733956117733957AG18GENIChomozygous116672236
8117734405117734406GT19GENIChomozygous117059336
8117734567117734568AG15GENIChomozygous117059338
8117735177117735178AT10GENIChomozygous117059340
8117735437117735438AG17GENIChomozygous117059342
8117735737117735738GT8GENIChomozygous117059344
8117736397117736398CT17GENIChomozygous117059346
8117736417117736418GA14GENIChomozygous117059348
8117736500117736501CT18GENIChomozygous117059350
8117736546117736547AT16GENIChomozygous117059352
8117737230117737231CT10GENIChomozygous117059353
8117738996117738997GA19GENIChomozygous117059355
8117739238117739239TC22GENIChomozygous116672250
8117740471117740472GA20GENIChomozygous117059356
8117740681117740682CT13GENIChomozygous117059357
8117741235117741236GA12GENIChomozygous117059359
8117742460117742461CT18GENIChomozygous117059360
8117743032117743033AG14GENIChomozygous116672272
8117743124117743125TC16GENIChomozygous116672274
8117743267117743268GA18GENIChomozygous117059362
8117744225117744226TA12GENIChomozygous117912580
8117744226117744227AC13GENIChomozygous116672278
8117744439117744440AG8GENIChomozygous117059363
8117744804117744805TG14GENIChomozygous116672280
8117744899117744900AG8GENIChomozygous117059365
8117745057117745058GA26GENIChomozygous117059367
8117745414117745415GA27GENIChomozygous117059368
8117745435117745436TC22GENIChomozygous116672282
8117747179117747180AT16GENIChomozygous116672286
8117747496117747497CT14GENIChomozygous117059371
8117747829117747830AG21GENIChomozygous117059373
8117747858117747859GA19GENIChomozygous117059375