chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124473723124473724AC7GENIChomozygous880442966
7124473882124473883CT19GENIChomozygous880442967
7124476979124476980AG10GENICheterozygous880442968
7124477222124477223GT14GENIChomozygous880442969
7124479267124479268CT10GENIChomozygous880442970
7124481146124481147CT8GENIChomozygous880442971
7124481242124481243GA16GENIChomozygous880442972
7124481581124481582GA12GENIChomozygous880442973
7124482145124482146TC8GENIChomozygous880442974
7124482410124482411AG9GENIChomozygous880442975
7124482804124482805CT11GENIChomozygous880442976
7124482851124482852GA12GENIChomozygous880442977
7124483065124483066GA14GENIChomozygous880442978
7124483197124483198CT8GENIChomozygous880442979
7124483201124483202GA5GENIChomozygous880442980
7124483364124483365AG14GENIChomozygous880442981
7124483457124483458CT11GENIChomozygous880442982
7124483730124483731CT8GENIChomozygous880442983
7124483749124483750GA6GENIChomozygous880442984
7124483761124483762TC5GENIChomozygous880442985
7124484943124484944TC11GENICheterozygous880442986
7124486185124486186GC20GENIChomozygous880442987
7124486252124486253AC22GENIChomozygous880442988
7124486398124486399AC9GENIChomozygous880442989
7124487212124487213GA15GENIChomozygous880442990
7124487574124487575TC16GENIChomozygous880442991
7124487701124487702TC10GENIChomozygous880442992
7124489115124489116TC16GENIChomozygous880442993
7124489229124489230AG9GENIChomozygous880442994
7124489497124489498CT14GENIChomozygous880442995
7124489541124489542CG11GENIChomozygous880442996
7124490103124490104AG14GENIChomozygous880442998