chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1593820715938208TC14GENIChomozygous45097830
X1593913715939138TC10GENIChomozygous45097831
X1594018115940182A-10GENIChomozygous45097832
X1594028515940287AC--9GENIChomozygous45097833
X1594048015940481GT11GENIChomozygous45097834
X1594104615941047TC13GENIChomozygous45097835
X1594132315941324TTTAAAAAGTAGATGGGGGCTGGAGAGATGGCTCAGCCGTTAAAGGCTAGGCTCACAACCAAAAATA21GENIChomozygous45501287
X1594212115942122GA10GENIChomozygous45097836
X1594241415942415AAAAAGAAAGAAAG4GENIChomozygous45628927
X1594270315942704C-7GENIChomozygous45097837
X1594271315942714G-8GENIChomozygous45097838
X1594272515942726CG7GENIChomozygous45252136
X1594276415942765GT8GENIChomozygous45097839
X1594285015942851TC3GENIChomozygous45097842
X1594440515944406TTG10GENICheterozygous45501289
X1594440815944409GGGGGCTCGAGACCCCAAAAGTACAAC10GENICheterozygous45501291
X1594479115944792TC16GENIChomozygous45097844
X1594480115944802GA14GENIChomozygous45097845
X1594485715944859AA--16GENICheterozygous45501293
X1594485815944859A-16GENICpossibly homozygous45501295
X1594495015944951CT12GENIChomozygous45097847
X1594528415945285G-15GENIChomozygous45097848
X1594652015946521CT12GENIChomozygous45097849