chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107946242107947GGT11GENIChomozygous61136169
1242107964242107965GGA7GENICpossibly homozygous61136170
1242108561242108562TC27GENIChomozygous61136171
1242109616242109617AG37GENIChomozygous61136172
1242109688242109689T-25GENIChomozygous61623885
1242112448242112449AAC11GENIChomozygous61136173
1242112822242112823GA27GENIChomozygous61136174
1242113547242113548CT23GENIChomozygous61136175
1242114398242114399AATC16GENIChomozygous61136176
1242114516242114517GGT1GENIChomozygous61136177
1242115682242115683CA37GENIChomozygous61136178
1242111893242111894GGA16GENICpossibly homozygous62205948
1242111737242111738GGCACACACA7GENIChomozygous62205946