chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139455044139455045CT30GENIChomozygous115937025
7139455055139455056CT28GENIChomozygous115937026
7139455683139455684GA27GENIChomozygous115937027
7139455751139455752TC22GENIChomozygous115937028
7139455846139455847AG26GENIChomozygous115937029
7139455914139455915GA37GENIChomozygous115937030
7139455934139455935AG38GENICpossibly homozygous115937031
7139456223139456224AG33GENIChomozygous115937032
7139456296139456297GA31GENIChomozygous115937033
7139456317139456318GA31GENIChomozygous115937034
7139456324139456325AG32GENIChomozygous115937035
7139456368139456369TC34GENIChomozygous115937036
7139456797139456798AG13GENIChomozygous115937037
7139459749139459750AG32GENIChomozygous115937038
7139460044139460045CT33GENIChomozygous115937039
7139461350139461351GC26GENIChomozygous115937040
7139461855139461856GA34GENIChomozygous115937041
7139466913139466914AG29GENIChomozygous115937043
7139466986139466987GC26GENIChomozygous115937044
7139467248139467249TC29GENIChomozygous115937045
7139467676139467677GT24GENIChomozygous115937046
7139470471139470472AG33GENIChomozygous115937047
7139471035139471036GT31GENICpossibly homozygous115937048
7139471960139471961AG43GENIChomozygous115937049
7139472710139472711AG23GENIChomozygous115937050
7139473875139473876CT25GENIChomozygous115937051
7139474998139474999TG22GENIChomozygous115937052
7139474999139475000TC22GENIChomozygous115937053
7139475125139475126AG38GENIChomozygous115937054
7139477972139477973AG20GENIChomozygous115937055
7139481854139481855TC14GENIChomozygous115937056
7139482265139482266CT29GENIChomozygous115937057
7139484139139484140CT15GENIChomozygous115937058