chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108903426689034267CG53GENIChomozygous51536515
108903426889034269CA53GENICpossibly homozygous51536516
108903431789034318AG45GENIChomozygous51731186
108903549689035497GGT44GENIChomozygous51731188
108903554789035548CT51GENICheterozygous51731190
108903554789035548CCTTTTCTTTTT41GENIChomozygous51731192
108903599589035996TC66GENIChomozygous51731194
108903609389036094GGCTTTA47GENIChomozygous51731196
108903621189036212GA60GENICpossibly homozygous51731198
108903622289036223GC61GENIChomozygous51731200
108903635189036354TTG---28GENIChomozygous51731202
108903638489036387TTT---27GENIChomozygous51731204
108903661989036620CCTT45GENIChomozygous51731206
108903705189037052GGT10GENIChomozygous51536517
108903711289037113AT22GENIChomozygous51731208
108903719989037200AG51GENIChomozygous51731210
108903747189037477AACAAC------24GENIChomozygous51731212
108903773789037738AT60GENIChomozygous51731214
108903800889038009TC57GENIChomozygous51731216
108903822289038223GA45GENICpossibly homozygous51731218
108903822589038226CT41GENICpossibly homozygous51731219
108903888489038885AG72GENIChomozygous51731221
108903945689039457AC46GENIChomozygous51731223
108903959689039597TC41GENIChomozygous51731225
108903960889039609CCTG42GENIChomozygous51731227
108903971389039714TTC15GENIChomozygous51731229
108903976789039768GA30GENICpossibly homozygous51731231
108903982189039822GA47GENIChomozygous51731233
108904066989040670TG67GENIChomozygous51731235
108904115889041159AG52GENIChomozygous51731237
108904119189041192AG50GENIChomozygous51731239
108904133189041332GA65GENIChomozygous51731241
108904145789041459TG--26GENIChomozygous51731243
108904148689041487AG33GENICpossibly homozygous51731245
108904152589041526TTTC31GENIChomozygous51731247
108904152789041528TC35GENICpossibly homozygous51731249
108904162389041624AG45GENIChomozygous51731251