chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57726583077265831TC16GENIChomozygous70714945
57726644477266445TG13GENIChomozygous70714948
57726866377268664GA20GENIChomozygous70714951
57726917077269171GA12GENIChomozygous70714954
57726936877269369GA18GENIChomozygous70714957
57727146277271463CT17GENIChomozygous70714960
57727387877273879CG17GENIChomozygous70714963
57727402777274028GA12GENIChomozygous70714966
57727759577277596CT29GENIChomozygous70714969
57728144977281450CT14GENIChomozygous70714972
57728188777281888CT29GENIChomozygous70714975
57728857477288575AG16GENIChomozygous70714980
57728870877288709CT21GENIChomozygous70714983
57729220177292202CT19GENIChomozygous70714986
57729375677293757GT4GENIChomozygous70715010
57729504477295045CT14GENICheterozygous70715013