chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045798744579875AG18GENIChomozygous109074755
2045814974581498CG23GENIChomozygous109074759
2045821194582120CT31GENIChomozygous109074763
2045826244582625CT17GENIChomozygous109233527
2045827214582722TA15GENIChomozygous109074765
2045828304582831GA18GENIChomozygous109074767
2045829564582957GT18GENIChomozygous109074769
2045829954582996GA23GENIChomozygous109074771
2045832574583258CT24GENIChomozygous109074773
2045835624583563GT16GENIChomozygous109074777
2045863384586339GA24GENIChomozygous109074781
2045865354586536TA20GENIChomozygous109074783
2045867244586725AG16GENIChomozygous109074789
2045868224586823GA14GENIChomozygous109296144
2045859464585947AG24GENIChomozygous109296142
2045877364587737TG18GENIChomozygous109296148
2045880804588081GA20GENIChomozygous109329588
2045881064588107GA25GENIChomozygous109329590
2045890254589026GA26GENIChomozygous109074793
2045894224589423TC10GENIChomozygous109074797
2045912214591222CT22GENIChomozygous109329592
2045917614591762GA29GENIChomozygous109329594