chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2132784307132784308TC19GENICpossibly homozygous59088131
2132784787132784788TC8GENICpossibly homozygous59088132
2132784844132784845CT15GENIChomozygous59088133
2132785582132785583GA21GENICpossibly homozygous59088134
2132786073132786076TTA---2GENIChomozygous59088135
2132786077132786078C-2GENIChomozygous59088136
2132786094132786095TC9GENIChomozygous59088137
2132786203132786204AG20GENIChomozygous59088138
2132786327132786328TC30GENIChomozygous59088139
2132786832132786833AG9GENICpossibly homozygous59088140
2132787147132787148TG9GENIChomozygous59088143
2132787328132787329TC17GENIChomozygous59088144
2132787430132787431GA18GENICpossibly homozygous59088145
2132788544132788545CT20GENIChomozygous59088146
2132788835132788836CA4GENIChomozygous59088147