chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57726583077265831TC19GENIChomozygous70714945
57726644477266445TG14GENIChomozygous70714948
57726866377268664GA26GENIChomozygous70714951
57726917077269171GA15GENIChomozygous70714954
57726936877269369GA19GENIChomozygous70714957
57727146277271463CT18GENIChomozygous70714960
57727387877273879CG23GENIChomozygous70714963
57727402777274028GA18GENIChomozygous70714966
57727759577277596CT24GENIChomozygous70714969
57728144977281450CT18GENIChomozygous70714972
57728188777281888CT25GENIChomozygous70714975
57728857477288575AG28GENIChomozygous70714980
57728870877288709CT30GENIChomozygous70714983
57729220177292202CT13GENIChomozygous70714986
57729375677293757GT12GENIChomozygous70715010
57729504477295045CT8GENICheterozygous70715013