chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118161056118161057TA33GENIChomozygous116673189
8118166915118166916CT34GENIChomozygous116673193
8118167052118167053TC32GENIChomozygous116673195
8118167649118167650TC31GENIChomozygous116673197
8118168620118168621GA30GENIChomozygous117059799
8118170343118170344GA26GENIChomozygous116673199
8118170544118170545AC34GENIChomozygous117059801
8118171107118171108AG22GENIChomozygous116673201
8118178403118178404AG20GENIChomozygous116673209
8118179554118179555GA15GENIChomozygous116673211
8118179605118179606AC26GENIChomozygous116673213
8118179766118179767GA21GENICpossibly homozygous116673215
8118181220118181221GA22GENIChomozygous117059803
8118181465118181466CT22GENIChomozygous117059805
8118182231118182232CT27GENIChomozygous116673217
8118186299118186300GT27GENIChomozygous116673221
8118186621118186622GA28GENIChomozygous117059807
8118190683118190684TC11GENIChomozygous116673225
8118190891118190892AG10GENIChomozygous116673227
8118190968118190969CG18GENIChomozygous116673229
8118191706118191707CG22GENIChomozygous116673231
8118193941118193942AC12GENIChomozygous116888069
8118193944118193945AC12GENIChomozygous116888071
8118193947118193948AC12GENIChomozygous116888073
8118193950118193951AC13GENIChomozygous116673233
8118193953118193954AC15GENIChomozygous116673235
8118194412118194413AG15GENIChomozygous116673239
8118194428118194429TG15GENIChomozygous117059809