chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110926766110926769TCT50GENIChomozygous138264670
8110926883110926884GA53GENIChomozygous138414857
8110927037110927038AG37GENIChomozygous138414858
8110927765110927766GA35GENIChomozygous138414859
8110928093110928094AG43GENIChomozygous138414860
8110928182110928183AG51GENIChomozygous138414861
8110928348110928349TG32GENIChomozygous138414862
8110928365110928366CT31GENIChomozygous138414863
8110928405110928406AG19GENIChomozygous138414864
8110928447110928448CG21GENIChomozygous138414865
8110928554110928555AG39GENIChomozygous138414866
8110928579110928579C46GENIChomozygous138264671
8110928674110928675TC52GENIChomozygous138414867
8110928711110928712AG48GENIChomozygous138414868
8110928943110928944AG46GENIChomozygous138414869
8110928958110928959CA43GENIChomozygous138414870
8110929201110929202AC52GENICpossibly homozygous138414871
8110929569110929570AG47GENIChomozygous138414872
8110929715110929716TC43GENIChomozygous138414873
8110929773110929774TC43GENIChomozygous138414874
8110929856110929857TG46GENIChomozygous138414875
8110929955110929956TG27GENIChomozygous138414876
8110930164110930165GA47GENIChomozygous138414877
8110930235110930236CT62GENIChomozygous138414878
8110930689110930690CG49GENIChomozygous138414879
8110930946110930947TA45GENIChomozygous138414880
8110930974110930975CA31GENIChomozygous138414881
8110931064110931065CA37GENICpossibly homozygous138414882
8110931109110931135GGGAGGCTTGAGTCTGTTTGAACTCA39GENIChomozygous138264675
8110928775110928775AC49GENIChomozygous138264672
8110929280110929310TACAGTTAATGTTTACGTTATTTGCACGTA49GENIChomozygous138264673
8110930955110930955AGGGAAACTGACA45GENIChomozygous138264674
8110931146110931147CA50GENIChomozygous138414883
8110931165110931166TC52GENIChomozygous138414884
8110931293110931294GT47GENIChomozygous138414885
8110935560110935561C42GENIChomozygous138264676
8110931829110931830TC57GENIChomozygous138414887
8110931451110931452AC54GENIChomozygous138414886