chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104423941344239414CA26GENIChomozygous116580886
104423987944239880CG27GENIChomozygous117077773
104424059844240599GC26GENIChomozygous116768096
104424083244240833CT27GENIChomozygous116768122
104424119344241194TC28GENIChomozygous116768148
104424171544241716AC22GENIChomozygous116768170
104424182244241823AG28GENIChomozygous117008111
104424210144242102CT34GENIChomozygous117008112
104424269344242694GA36GENICpossibly homozygous117077774
104424272644242727GA37GENICpossibly homozygous117077775
104424277344242774TC37GENICpossibly homozygous117008113