chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045798744579875AG7GENIChomozygous109074755
2045819864581987GA20GENIChomozygous109074761
2045821194582120CT15GENIChomozygous109074763
2045827214582722TA12GENIChomozygous109074765
2045828304582831GA18GENIChomozygous109074767
2045829564582957GT17GENIChomozygous109074769
2045829954582996GA15GENIChomozygous109074771
2045832574583258CT23GENIChomozygous109074773
2045834684583469CA11GENIChomozygous109074775
2045835624583563GT11GENICpossibly homozygous109074777
2045863384586339GA7GENIChomozygous109074781
2045865354586536TA10GENIChomozygous109074783
2045867244586725AG4GENIChomozygous109074789
2045868224586823GA7GENIChomozygous109296144
2045877364587737TG13GENIChomozygous109296148
2045880804588081GA15GENIChomozygous109329588
2045881064588107GA22GENIChomozygous109329590
2045890254589026GA14GENIChomozygous109074793
2045894224589423TC5GENIChomozygous109074797
2045917614591762GA13GENIChomozygous109329594