chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137908012479080125TC48GENIChomozygous114402581
137908062779080628CA65GENIChomozygous114402583
137908137579081376TC55GENIChomozygous114402585
137908323379083234TC50GENIChomozygous114402587
137908356379083564TA50GENIChomozygous114402591
137908470379084704CT68GENIChomozygous114402593
137908533079085331GA59GENIChomozygous114402595
137908729279087293GT49GENIChomozygous114402597
137908744879087449CT66GENICpossibly homozygous114402599