chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC32GENIChomozygous117059332
8117733691117733692CT32GENIChomozygous117059334
8117733956117733957AG29GENIChomozygous116672236
8117734405117734406GT35GENIChomozygous117059336
8117734567117734568AG34GENIChomozygous117059338
8117735177117735178AT40GENIChomozygous117059340
8117735437117735438AG33GENIChomozygous117059342
8117735737117735738GT32GENIChomozygous117059344
8117736397117736398CT30GENIChomozygous117059346
8117736417117736418GA35GENIChomozygous117059348
8117736500117736501CT32GENIChomozygous117059350
8117736546117736547AT34GENIChomozygous117059352
8117737230117737231CT44GENIChomozygous117059353
8117738996117738997GA29GENIChomozygous117059355
8117739238117739239TC31GENIChomozygous116672250
8117740386117740387AG30GENIChomozygous116672256
8117740471117740472GA25GENIChomozygous117059356
8117740681117740682CT42GENIChomozygous117059357
8117741235117741236GA39GENIChomozygous117059359
8117742119117742120TC50GENIChomozygous116672264
8117742460117742461CT34GENIChomozygous117059360
8117743032117743033AG32GENIChomozygous116672272
8117743124117743125TC42GENIChomozygous116672274
8117743267117743268GA47GENIChomozygous117059362
8117744226117744227AC46GENIChomozygous116672278
8117744439117744440AG44GENIChomozygous117059363
8117744804117744805TG32GENIChomozygous116672280
8117744899117744900AG45GENIChomozygous117059365
8117745057117745058GA44GENIChomozygous117059367
8117745414117745415GA30GENIChomozygous117059368
8117745435117745436TC29GENIChomozygous116672282
8117747179117747180AT30GENIChomozygous116672286
8117747496117747497CT35GENIChomozygous117059371
8117747829117747830AG38GENIChomozygous117059373
8117747858117747859GA36GENIChomozygous117059375
8117744225117744226TA44GENIChomozygous117912580