chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107946242107947GGT9GENIChomozygous61136169
1242107964242107965GGA10GENIChomozygous61136170
1242108561242108562TC38GENIChomozygous61136171
1242109616242109617AG45GENIChomozygous61136172
1242112448242112449AAC21GENIChomozygous61136173
1242112822242112823GA35GENIChomozygous61136174
1242113547242113548CT43GENIChomozygous61136175
1242114398242114399AATC25GENIChomozygous61136176
1242114516242114517GGT14GENICpossibly homozygous61136177
1242115682242115683CA45GENIChomozygous61136178