chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107946242107947GGT11GENIChomozygous61136169
1242107964242107965GGA11GENICheterozygous61136170
1242108561242108562TC15GENIChomozygous61136171
1242109616242109617AG27GENIChomozygous61136172
1242112448242112449AAC4GENIChomozygous61136173
1242112822242112823GA26GENIChomozygous61136174
1242113547242113548CT26GENIChomozygous61136175
1242114398242114399AATC16GENIChomozygous61136176
1242114516242114517GGT6GENICheterozygous61136177
1242115682242115683CA22GENIChomozygous61136178
1242109688242109689T-1GENIChomozygous61623885