chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57726583077265831TC42GENIChomozygous70714945
57726644477266445TG40GENIChomozygous70714948
57726801577268016GA29GENICheterozygous71917705
57726866377268664GA28GENIChomozygous70714951
57726917077269171GA13GENIChomozygous70714954
57726936877269369GA36GENIChomozygous70714957
57727146277271463CT47GENIChomozygous70714960
57727387877273879CG34GENIChomozygous70714963
57727402777274028GA33GENIChomozygous70714966
57727759577277596CT31GENIChomozygous70714969
57728144977281450CT18GENIChomozygous70714972
57728188777281888CT32GENIChomozygous70714975
57728233877282339GA15GENICheterozygous70714977
57728533577285336AT19GENICheterozygous71917708
57728857477288575AG41GENIChomozygous70714980
57728870877288709CT23GENIChomozygous70714983
57729220177292202CT32GENIChomozygous70714986
57729253077292531AG21GENICheterozygous70714989
57729253577292536CT25GENIChomozygous70714992
57729266477292665TA81GENICheterozygous70714998
57729267077292671GT77GENICheterozygous70715001
57729275877292759AG57GENICheterozygous70715007
57729375677293757GT23GENIChomozygous70715010
57729504477295045CT37GENICheterozygous70715013