chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC27GENIChomozygous117059332
8117733691117733692CT16GENIChomozygous117059334
8117733956117733957AG28GENIChomozygous116672236
8117734405117734406GT31GENIChomozygous117059336
8117734567117734568AG27GENIChomozygous117059338
8117735177117735178AT14GENIChomozygous117059340
8117735437117735438AG17GENIChomozygous117059342
8117736397117736398CT27GENIChomozygous117059346
8117736417117736418GA25GENIChomozygous117059348
8117736500117736501CT23GENIChomozygous117059350
8117736546117736547AT29GENIChomozygous117059352
8117737230117737231CT20GENIChomozygous117059353
8117738996117738997GA23GENIChomozygous117059355
8117739238117739239TC26GENIChomozygous116672250
8117740386117740387AG15GENIChomozygous116672256
8117740471117740472GA28GENIChomozygous117059356
8117740681117740682CT31GENIChomozygous117059357
8117741235117741236GA30GENIChomozygous117059359
8117743032117743033AG24GENIChomozygous116672272
8117743124117743125TC21GENIChomozygous116672274
8117743267117743268GA31GENIChomozygous117059362
8117744226117744227AC25GENIChomozygous116672278
8117744439117744440AG15GENIChomozygous117059363
8117744804117744805TG31GENIChomozygous116672280
8117744899117744900AG29GENIChomozygous117059365
8117745057117745058GA41GENIChomozygous117059367
8117745414117745415GA30GENIChomozygous117059368
8117745435117745436TC30GENIChomozygous116672282
8117747179117747180AT21GENIChomozygous116672286
8117747496117747497CT22GENIChomozygous117059371
8117747829117747830AG42GENIChomozygous117059373
8117747858117747859GA38GENIChomozygous117059375
8117744225117744226TA20GENIChomozygous117912580