chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118461614184616142AC49GENIChomozygous116107097
118461672184616722GT8GENICpossibly homozygous118167342
118461809684618097GA101GENICheterozygous118167343
118461811684618117AG167GENICheterozygous118167344
118461816484618165AG201GENICheterozygous118187641
118461816684618167GA194GENICheterozygous118187642
118461819184618192GA118GENICheterozygous118187643
118461832084618321AG62GENICheterozygous118187644
118461832884618329AG70GENICheterozygous118187645
118461833284618333AG72GENICheterozygous118187646
118461834084618341AG77GENICheterozygous118187647
118462914184629142CT59GENICheterozygous118187648
118462914384629144GC58GENICheterozygous118187649
118462915084629151AT63GENICheterozygous118187650
118462915284629153GT65GENICheterozygous118187651
118462920084629201AG92GENICheterozygous118187652
118462920284629203TC91GENICheterozygous118187653
118462921284629213TA82GENICheterozygous118187654
118462922584629226AG80GENICheterozygous118187655
118463971384639714CA59GENICheterozygous118187656
118463972084639721TC64GENICheterozygous118187657
118463972984639730AC63GENICheterozygous118187658
118463978384639784TC77GENICheterozygous118187659
118463968184639682AG67GENIChomozygous115998062