chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X21267072126708AG9GENIChomozygous45076473
X21280452128046TTC7GENICpossibly homozygous45076474
X21287932128794CT15GENIChomozygous45076475
X21312352131239AAAC----12GENIChomozygous45076476
X21314122131413GGT9GENIChomozygous45076477