chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109099086390990864AG42GENIChomozygous116905141
109099099490990995CG54GENIChomozygous116905143
109099116290991163CT43GENIChomozygous116905145
109099117590991175CGGCGGT42GENIChomozygous131708921
109099118590991186TC41GENIChomozygous116905147
109099118990991190CA37GENIChomozygous116905149
109099119090991191AG38GENIChomozygous116905151
109099145590991456TC53GENIChomozygous116905153
109099155590991556CG49GENIChomozygous116905155
109099174390991744TA63GENIChomozygous116905157
109099213990992140TC52GENICpossibly homozygous116821482
109099215190992152AC55GENICpossibly homozygous116905159
109099230490992305GC31GENIChomozygous116905161
109099316990993170GA40GENIChomozygous116905163
109099324690993246ACTAGT45GENIChomozygous131708922
109099333690993337AG46GENIChomozygous116905165
109099360690993607CG41GENIChomozygous116905167
109099392190993922GA43GENIChomozygous117020578
109099418490994185GA33GENIChomozygous116905169
109099460190994601AT15GENIChomozygous131708923
109099480390994804GA40GENIChomozygous116821488
109099494190994941TG28GENIChomozygous131708924
109099494390994944CT30GENIChomozygous123403776
109099497790994978CT33GENIChomozygous123403777
109099518690995187GA42GENIChomozygous116905171
109099572390995724AG50GENIChomozygous116821490
109099582790995828TC39GENIChomozygous116821492
109099675390996754TC47GENIChomozygous116821494
109099742490997425AG33GENIChomozygous116821496
109099800990998010AC19GENIChomozygous116905173
109099801290998012CTGCG19GENIChomozygous128844847
109099461190994612AT17GENIChomozygous117068573
109099650590996505A39GENIChomozygous128844845
109099800290998007GAGAG19GENIChomozygous128844846
109099803390998034GC13GENIChomozygous116905175
109099824390998244AG43GENIChomozygous116821498
109099875390998754TA61GENIChomozygous116905177
109099887990998880CT41GENIChomozygous116821507
109099923190999232AG48GENIChomozygous116821509