chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1273219070273219071AG12GENIChomozygous61646226
1273219071273219072AG14GENIChomozygous61646227
1273220368273220369TC7GENIChomozygous61224007
1273220445273220446CA12GENIChomozygous61646229
1273221362273221363TTA13GENIChomozygous61224008
1273222839273222840CA7GENIChomozygous61646232
1273222840273222841CA7GENIChomozygous61646233
1273224559273224560GGA14GENIChomozygous61646234
1273225013273225014AACG15GENICpossibly homozygous61224011
1273226372273226373C-18GENIChomozygous61646235
1273226899273226913ACACACACACACAC--------------6GENIChomozygous61646236
1273227560273227562GG--10GENIChomozygous61684565
1273227820273227822GA--8GENIChomozygous61646237