chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124247957242479573TC1GENIChomozygous50209155
124248395142483952G-2GENICheterozygous50209157
124248470742484708CT16GENIChomozygous50209161
124248766542487666AC9GENIChomozygous50209167
124248770642487707CT14GENICpossibly homozygous50209168
124248772942487730TC15GENIChomozygous50209169
124248897242488973GA27GENIChomozygous50209174
124249034742490348TA20GENIChomozygous50209175
124249053842490539AG27GENIChomozygous50209176
124249065742490658CT30GENIChomozygous50209180
124249355242493553CT6INTERGENICheterozygous50592218
124249410142494102CA15INTERGENIChomozygous50209183
124249415742494158AG21INTERGENIChomozygous50209184