chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107964242107965GGA6GENICheterozygous754723158
1242107979242107980CA9GENIChomozygous646033225
1242108561242108562TC21GENIChomozygous646033226
1242109100242109101GA9GENIChomozygous646033227
1242109190242109191GA7GENIChomozygous646033228
1242109616242109617AG31GENIChomozygous646033229
1242109687242109688CCTT24GENIChomozygous754723160
1242111738242111748CACACACACA----------10GENIChomozygous754723161
1242111893242111894GGA6GENICheterozygous754723165
1242112448242112449AAC3GENIChomozygous754723166
1242113268242113269CA26GENIChomozygous646033230
1242113547242113548CT15GENICpossibly homozygous646033231
1242114398242114399AATC16GENIChomozygous754723167
1242114516242114517GGT7GENICheterozygous754723168
1242114516242114517GGTT7GENICheterozygous754723169
1242115682242115683CA5GENIChomozygous646033232