chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2132784307132784308TC28GENIChomozygous59088131
2132785326132785327TA13GENIChomozygous61394943
2132786327132786328TC37GENICpossibly homozygous59088139
2132786433132786434GA34GENIChomozygous61394945
2132786832132786833AG20GENIChomozygous59088140
2132786909132786910GGCC3GENIChomozygous61394947
2132787082132787086GAAG----4GENIChomozygous61394949
2132787147132787148TG32GENIChomozygous59088143
2132787328132787329TC30GENIChomozygous59088144
2132787430132787431GA23GENIChomozygous59088145
2132788544132788545CT24GENIChomozygous59088146