chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116479140564791406TG4GENIChomozygous115883212
116479319564793196AG16GENIChomozygous115883214
116479327464793275CT11GENIChomozygous115883216
116479327764793278AT9GENIChomozygous115883218
116479539864795399AC19GENIChomozygous115883220
116479571064795711CT15GENIChomozygous115883222
116479596664795967AT21GENIChomozygous115883224
116479600564796006GC16GENIChomozygous115883226
116479626164796262TA12GENIChomozygous115883228
116479641364796414CG10GENIChomozygous115883230
116479644164796442CT13GENIChomozygous115883232
116479682864796829GT21GENIChomozygous115883234
116479765664797657TC13GENIChomozygous115883236
116479853364798534CT28GENIChomozygous116104978
116479893364798934TG17GENIChomozygous115883238
116479955964799560TC18GENIChomozygous115883240
116480226564802266TC3GENICheterozygous115883244
116480237364802374AC17GENIChomozygous115883246
116480248964802490GA17GENIChomozygous115883248
116480316364803164TC9GENIChomozygous116110416
116480363864803639AG16GENIChomozygous115883250
116480376764803768AG16GENIChomozygous115883252
116480414564804146GA9GENIChomozygous115883254
116480465364804654TC14GENIChomozygous115883256
116480501064805011TC7GENIChomozygous115883258
116480790164807902CT16GENIChomozygous115883270
116480803364808034AG12GENIChomozygous115883272
116480829564808296TG20GENIChomozygous115883274
116480873564808736CT12GENIChomozygous115883277
116480890964808910TC14GENIChomozygous115883279