chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1593913715939138TC9GENIChomozygous45097831
X1594212115942122GA17GENIChomozygous45097836
X1594213515942136GA17GENIChomozygous45274087
X1594230115942302AAT10GENIChomozygous45274088
X1594231315942314AG9GENIChomozygous45274089
X1594270315942704C-3GENIChomozygous45097837
X1594271315942714G-3GENIChomozygous45097838
X1594479715944798AG15GENICpossibly homozygous45274091
X1594276415942765GT5GENIChomozygous45097839
X1594279015942791TG5GENIChomozygous45097840
X1594280015942801TC8GENIChomozygous45097841
X1594285015942851TC11GENIChomozygous45097842
X1594343115943432CT22GENIChomozygous45274090
X1594272515942726CG3GENIChomozygous45252136
X1594480115944802GA16GENICpossibly homozygous45097845
X1594495015944951CT14GENIChomozygous45097847
X1594596215945968TTAAAG------6GENICheterozygous45274092