chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1491909914919100CT10GENIChomozygous144505218
X1492275514922756AG10GENIChomozygous144505219
X1492320214923203TC14GENIChomozygous144505220
X1492392014923920T15GENICpossibly homozygous144502153
X1492465614924657CT9GENIChomozygous144505221
X1492492514924926CT9GENIChomozygous144505222