chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137907870779078717TATGTATCTA10GENIChomozygous129076967
137908264779082649TA12GENIChomozygous129076968
137908137579081376TC23GENIChomozygous114402585
137908356279083563AG15GENIChomozygous114402589
137908012479080125TC14GENICpossibly homozygous114402581
137908062779080628CA25GENIChomozygous114402583
137908323379083234TC17GENIChomozygous114402587
137908356379083564TA15GENIChomozygous114402591
137908470379084704CT26GENIChomozygous114402593
137908533079085331GA33GENIChomozygous114402595
137908615479086154ACC18GENIChomozygous129076969
137908651179086516CCCCA21GENIChomozygous129076970
137908729279087293GT22GENIChomozygous114402597
137908744879087449CT18GENIChomozygous114402599