chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887405140887406GC11GENIChomozygous879841745
4140887526140887527AG14GENIChomozygous879841746
4140889290140889291CA8GENIChomozygous879841747
4140892114140892115TA17GENIChomozygous879841748
4140894149140894150GA16GENIChomozygous879841749
4140894658140894659GC19GENICpossibly homozygous879841750
4140895511140895512GT5GENIChomozygous879841751
4140896988140896989GA14GENIChomozygous879841752
4140899328140899329GA22GENIChomozygous879841753
4140901019140901020TC6GENICheterozygous879841754
4140903807140903808CT27GENIChomozygous879841755
4140906395140906396AG4GENIChomozygous879841756
4140907775140907776TG18GENIChomozygous879841757
4140908274140908275TG25GENIChomozygous879841758
4140908994140908995GC19GENIChomozygous879841759
4140909042140909043GA17GENIChomozygous879841760
4140909059140909060CA16GENIChomozygous879841761
4140909109140909110GA8GENIChomozygous879841762
4140909129140909130CT12GENIChomozygous879841763
4140909170140909171GA9GENIChomozygous879841764
4140909196140909197CT9GENIChomozygous879841765
4140909244140909245GT5GENIChomozygous879841766
4140909248140909249TA5GENIChomozygous879841767
4140909269140909270GA6GENICheterozygous879841768
4140909286140909287GC10GENICheterozygous879841769
4140916630140916631TG12GENIChomozygous879841770
4140916631140916632CA12GENIChomozygous879841771
4140916937140916938GA12GENIChomozygous879841772