chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104892964948929650CT29GENIChomozygous117129363
104892986348929864AG30GENIChomozygous116881234
104893001248930013AG27GENIChomozygous116881236
104893024948930250CA14GENIChomozygous117129365
104893046648930467AG16GENIChomozygous116881238
104893052748930528CT19GENIChomozygous116881240
104893105348931054TC24GENIChomozygous116881242
104893158848931589GA17GENIChomozygous117009339
104893163448931635CG19GENIChomozygous116881246
104893186348931864TC13GENIChomozygous117009340
104893229848932299GA18GENIChomozygous116881248
104893246248932463GA18GENIChomozygous116881250
104893302148933022CT20GENIChomozygous116881252
104893367948933680AG23GENIChomozygous116881254
104893369148933692CA26GENIChomozygous117129367
104893417948934180TC21GENIChomozygous116881256
104893470548934706CT11GENIChomozygous117009341
104893564248935643AG22GENIChomozygous116881264
104893611448936115TA13GENIChomozygous117129369
104893612348936124AT13GENIChomozygous117129371
104893700948937010AG19GENIChomozygous116881270
104893755848937559CT17GENIChomozygous116881272
104893803148938032TC22GENIChomozygous117129373
104893988048939881AG26GENIChomozygous116881274
104894064448940645CT16GENIChomozygous116881276
104894077448940775GA17GENIChomozygous117129375
104894170048941701GC21GENIChomozygous117129377
104894273948942740CT15GENIChomozygous117129381
104894303748943038CT25GENIChomozygous117129383
104894358248943583AG12GENIChomozygous116881285
104894389748943898CG13GENIChomozygous116881287
104894425148944252AG18GENIChomozygous116881289
104894465548944656AG12GENIChomozygous116881291
104894485248944853GA20GENIChomozygous117129385
104894566448945665TC19GENIChomozygous116881299
104894582148945822TC29GENIChomozygous117009352
104894618348946184AG30GENIChomozygous116881303
104894630248946303CA19GENIChomozygous116881305
104894719548947196GA18GENIChomozygous117129389
104894734348947344TC24GENIChomozygous116881309
104894749848947499AG25GENIChomozygous116881311