chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104407664744076648CT10GENIChomozygous576629345
104407799544077996AACTCTCTCT2GENIChomozygous715061357
104408046744080468GGT15GENICpossibly homozygous715061358
104408301544083016CT23GENIChomozygous603980768
104408330344083304TC24GENIChomozygous603980769
104408344744083448A-14GENIChomozygous715061359
104408345244083453C-16GENIChomozygous715061360
104408371144083712CA4GENIChomozygous603980770
104408620544086206G-9GENIChomozygous715061361
104408621044086211AC10GENIChomozygous603980771
104408621544086216AC9GENIChomozygous603980772
104408746144087462AG13GENIChomozygous603980773