chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139455044139455045CT29GENIChomozygous115937025
7139455055139455056CT27GENIChomozygous115937026
7139455683139455684GA26GENIChomozygous115937027
7139455751139455752TC20GENIChomozygous115937028
7139455846139455847AG26GENIChomozygous115937029
7139455914139455915GA35GENIChomozygous115937030
7139455934139455935AG36GENICpossibly homozygous115937031
7139456223139456224AG33GENIChomozygous115937032
7139456296139456297GA30GENIChomozygous115937033
7139456317139456318GA30GENIChomozygous115937034
7139456324139456325AG31GENIChomozygous115937035
7139456797139456798AG12GENIChomozygous115937037
7139459749139459750AG31GENIChomozygous115937038
7139460044139460045CT32GENIChomozygous115937039
7139461350139461351GC26GENIChomozygous115937040
7139461855139461856GA32GENIChomozygous115937041
7139466913139466914AG27GENIChomozygous115937043
7139466986139466987GC26GENIChomozygous115937044
7139467248139467249TC29GENIChomozygous115937045
7139467676139467677GT24GENIChomozygous115937046
7139470471139470472AG29GENIChomozygous115937047
7139471035139471036GT29GENIChomozygous115937048
7139471960139471961AG42GENIChomozygous115937049
7139472710139472711AG23GENIChomozygous115937050
7139473126139473127GT26GENIChomozygous118260887
7139473875139473876CT24GENIChomozygous115937051
7139474998139474999TG23GENIChomozygous115937052
7139474999139475000TC23GENIChomozygous115937053
7139475125139475126AG36GENIChomozygous115937054
7139475529139475530TA14GENIChomozygous118260889
7139477972139477973AG19GENIChomozygous115937055
7139481854139481855TC14GENIChomozygous115937056
7139482265139482266CT31GENIChomozygous115937057
7139484139139484140CT14GENIChomozygous115937058