chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117733610117733611AC22GENIChomozygous117059332
8117733691117733692CT26GENIChomozygous117059334
8117733956117733957AG28GENIChomozygous116672236
8117734405117734406GT47GENIChomozygous117059336
8117734567117734568AG32GENIChomozygous117059338
8117735177117735178AT21GENIChomozygous117059340
8117735437117735438AG26GENIChomozygous117059342
8117735737117735738GT15GENIChomozygous117059344
8117736397117736398CT18GENIChomozygous117059346
8117736417117736418GA17GENIChomozygous117059348
8117736500117736501CT20GENIChomozygous117059350
8117736546117736547AT20GENIChomozygous117059352
8117737230117737231CT15GENIChomozygous117059353
8117739238117739239TC23GENIChomozygous116672250
8117740386117740387AG20GENIChomozygous116672256
8117740471117740472GA26GENIChomozygous117059356
8117740681117740682CT24GENIChomozygous117059357
8117741235117741236GA23GENIChomozygous117059359
8117742460117742461CT15GENIChomozygous117059360
8117743032117743033AG25GENIChomozygous116672272
8117743124117743125TC26GENIChomozygous116672274
8117743267117743268GA35GENIChomozygous117059362
8117744226117744227AC29GENIChomozygous116672278
8117744439117744440AG32GENIChomozygous117059363
8117744804117744805TG29GENIChomozygous116672280
8117744899117744900AG33GENIChomozygous117059365
8117745057117745058GA34GENIChomozygous117059367
8117745414117745415GA37GENIChomozygous117059368
8117745435117745436TC39GENIChomozygous116672282
8117747179117747180AT18GENIChomozygous116672286
8117747496117747497CT37GENIChomozygous117059371
8117747829117747830AG32GENIChomozygous117059373
8117747858117747859GA19GENIChomozygous117059375