chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X118728126118728127GT14GENIChomozygous108316647
X118734195118734196CT11GENIChomozygous108316651
X118736194118736195AG10GENIChomozygous108316653
X118743458118743459CT13GENIChomozygous108316658
X118744367118744368TC5GENIChomozygous108316660
X118745427118745428CA5GENIChomozygous108316662
X118747434118747435CT17GENIChomozygous108316664
X118750741118750742CA7GENIChomozygous108419910
X118755357118755358TA13GENIChomozygous108316666
X118757041118757042TA11GENIChomozygous108316668
X118757042118757043AG11GENIChomozygous108316670
X118757164118757165GT9GENIChomozygous108316672
X118763192118763193AT15GENIChomozygous108316674
X118766238118766239TC10GENIChomozygous108316676