chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136547637136547638AC11GENIChomozygous56941245
4136548241136548242GA27GENICpossibly homozygous56941246
4136548500136548501AC19GENIChomozygous56941247
4136548641136548642AAT9GENICpossibly homozygous56941248
4136548642136548643AAGCAG9GENICpossibly homozygous56941249
4136548806136548807TC18GENICpossibly homozygous56941250
4136550467136550468AG15GENICpossibly homozygous56941256
4136550975136550976CG13GENIChomozygous56941260
4136551479136551480AG20GENICpossibly homozygous56941261
4136553426136553427TC9GENICpossibly homozygous56941262