chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728380217283803TG37GENIChomozygous930237246
141728481617284817CT42GENIChomozygous930237247
141728489917284900CT53GENIChomozygous930237248
141728505217285053TA40GENIChomozygous930237249
141728505817285059CT40GENIChomozygous930237250
141728520317285204GC37GENIChomozygous930237251
141728529317285294TG18GENIChomozygous930237252
141728563217285633CT55GENIChomozygous930237253
141728587617285877CG43GENIChomozygous930237254
141728588117285882CT39GENIChomozygous930237255
141728645617286457TC50GENIChomozygous930237256
141728669517286696CT38GENIChomozygous930237257
141728676817286769TA38GENIChomozygous930237258
141728677617286777TC35GENIChomozygous930237259
141728685817286859TC34GENIChomozygous930237260
141728703617287037CA30GENIChomozygous930237261
141728710317287104CT19GENIChomozygous930237262
141728936117289362AT34GENIChomozygous930237263
141729113417291135GA39GENIChomozygous930237264
141729148217291483GC36GENIChomozygous930237265
141729201917292020CT53GENIChomozygous930237266
141729228617292287GC48GENIChomozygous930237267
141729295017292951CT40GENIChomozygous930237268
141729299117292992TC34GENIChomozygous930237269
141729314017293141GA33GENIChomozygous930237270
141729327917293280AC35GENIChomozygous930237271
141729329117293292TC26GENIChomozygous930237272
141729348817293489AG44GENIChomozygous930237273
141729472117294722AG51GENIChomozygous930237274
141729490717294908AG34GENIChomozygous930237275
141729502417295025TC30GENIChomozygous930237276
141729540917295410CT44GENIChomozygous930237277
141729542117295422GA46GENICpossibly homozygous930237278
141729553717295538TC23GENIChomozygous930237279
141729591217295913TC33GENIChomozygous930237280
141729593717295938AG41GENIChomozygous930237281
141729638517296386AG49GENIChomozygous930237282
141729972117299722AG47GENIChomozygous930237283
141730108917301090TG54GENIChomozygous930237284
141730127317301274TC41GENIChomozygous930237285