chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1273219070273219071AG48GENIChomozygous61646226
1273219071273219072AG49GENICpossibly homozygous61646227
1273220153273220154TTAAAA9GENIChomozygous61646228
1273220169273220170GA35GENICheterozygous61684564
1273220368273220369TC33GENICheterozygous61224007
1273220445273220446CA16GENICpossibly homozygous61646229
1273221362273221363TTA27GENIChomozygous61224008
1273221463273221464AAG13GENICheterozygous61646230
1273221463273221464AAGG13GENICheterozygous61646231
1273222839273222840CA3GENIChomozygous61646232
1273222840273222841CA3GENIChomozygous61646233
1273224559273224560GGA19GENIChomozygous61646234
1273225013273225014AACG44GENIChomozygous61224011
1273226372273226373C-33GENIChomozygous61646235
1273226899273226913ACACACACACACAC--------------8GENICpossibly homozygous61646236
1273227560273227562GG--20GENICheterozygous61684565
1273227561273227562G-20GENICpossibly homozygous61224014
1273227820273227822GA--28GENIChomozygous61646237
1273228017273228018A-15GENIChomozygous61646238