chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118161056118161057TA33GENIChomozygous116673189
8118166915118166916CT28GENIChomozygous116673193
8118167649118167650TC22GENICpossibly homozygous116673197
8118170343118170344GA21GENIChomozygous116673199
8118171107118171108AG19GENIChomozygous116673201
8118178403118178404AG21GENIChomozygous116673209
8118179554118179555GA22GENIChomozygous116673211
8118179605118179606AC27GENIChomozygous116673213
8118182231118182232CT29GENIChomozygous116673217
8118186299118186300GT21GENIChomozygous116673221
8118168620118168621GA19GENIChomozygous117059799
8118170544118170545AC22GENIChomozygous117059801
8118181220118181221GA31GENIChomozygous117059803
8118181465118181466CT24GENIChomozygous117059805
8118186621118186622GA26GENICpossibly homozygous117059807
8118190683118190684TC38GENICpossibly homozygous116673225
8118190891118190892AG25GENIChomozygous116673227
8118190968118190969CG25GENIChomozygous116673229
8118191706118191707CG23GENIChomozygous116673231
8118194412118194413AG32GENIChomozygous116673239
8118194428118194429TG27GENIChomozygous117059809