chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57726583077265831TC35GENIChomozygous70714945
57726644477266445TG55GENICpossibly homozygous70714948
57726866377268664GA40GENIChomozygous70714951
57726917077269171GA21GENIChomozygous70714954
57726936877269369GA39GENIChomozygous70714957
57727146277271463CT46GENIChomozygous70714960
57727387877273879CG78GENICpossibly homozygous70714963
57727402777274028GA44GENIChomozygous70714966
57727759577277596CT46GENIChomozygous70714969
57728144977281450CT53GENIChomozygous70714972
57728188777281888CT46GENIChomozygous70714975
57728233877282339GA48GENICheterozygous70714977
57728857477288575AG53GENIChomozygous70714980
57728870877288709CT56GENIChomozygous70714983
57729220177292202CT42GENIChomozygous70714986
57729253077292531AG13GENICheterozygous70714989
57729253577292536CT19GENIChomozygous70714992
57729253777292538TG23GENICheterozygous70714995
57729266477292665TA48GENICheterozygous70714998
57729267077292671GT45GENICheterozygous70715001
57729272877292729AG52GENICheterozygous70715004
57729275877292759AG71GENICheterozygous70715007
57729375677293757GT27GENIChomozygous70715010
57729504477295045CT27GENICheterozygous70715013