chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X105406445105406446CT28GENIChomozygous108528155
X105406546105406547A19GENICpossibly homozygous134763140
X105406570105406571TA19GENIChomozygous108733776
X105409636105409637GA30GENIChomozygous108733778
X105411408105411409AT23GENIChomozygous108733780
X105411666105411667A20GENIChomozygous133695522
X105411724105411725TC27GENIChomozygous108528157
X105411909105411910GC29GENIChomozygous108733782
X105412847105412848AG27GENIChomozygous108733784
X105416174105416174TT22GENICpossibly homozygous134763142
X105416183105416184CT22GENICpossibly homozygous130808206
X105409062105409062AA32GENIChomozygous129776334
X105414460105414461AG25GENIChomozygous134979514