chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18242483482424835AG11GENIChomozygous108878096
18242600182426002AG14GENIChomozygous108878097
18242771082427711CT3GENIChomozygous108878100
18242873982428740CT14GENIChomozygous108878101
18242891282428913AG9GENIChomozygous120481877
18242940882429409CT11GENIChomozygous108878102
18243036282430363TG10GENIChomozygous108878103
18243218882432189CT14GENIChomozygous120481878
18243283182432832AC8GENIChomozygous108878105
18243317482433175GA11GENIChomozygous108878107
18243779982437800TC9GENIChomozygous108878116
18243789882437899GT9GENIChomozygous120481879
18243813882438139GA12GENIChomozygous120481880
18243857882438579AG5GENIChomozygous108878117
18243886782438868TC4GENIChomozygous108878118
18244006182440062CT7GENIChomozygous120481881
18244126382441264AT3GENIChomozygous120481882
18244126582441266AT3GENIChomozygous120481883
18244126782441268AT4GENICheterozygous120481884
18244137082441371TC7GENIChomozygous108878123
18244232882442329TC14GENIChomozygous120481885
18244248782442488GA4GENIChomozygous108878126
18244448682444487CT7GENIChomozygous120481886
18244469182444692TC6GENIChomozygous108878130
18244499682444997CT11GENIChomozygous109302474
18244549282445493TC14GENIChomozygous108878132
18244724182447242TG8GENIChomozygous108878147
18244785582447856GC8GENIChomozygous108878148
18244807382448074AG15GENIChomozygous120481887
18244808082448081AG15GENIChomozygous108878149
18244810982448110CT17GENIChomozygous108878150
18244821882448219CT7GENIChomozygous108878151
18244824382448244TG8GENIChomozygous108878152
18244969882449699CA4GENIChomozygous108878155
18244971182449712AC5GENIChomozygous108878156
18244985882449859AC15GENIChomozygous108878157
18245179482451795CT18GENIChomozygous108878158
18245197082451971CT9GENIChomozygous109302508