chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118161056118161057TA10GENIChomozygous116673189
8118166915118166916CT15GENIChomozygous116673193
8118167649118167650TC9GENIChomozygous116673197
8118168620118168621GA22GENIChomozygous117059799
8118170343118170344GA11GENIChomozygous116673199
8118170544118170545AC23GENIChomozygous117059801
8118171107118171108AG23GENIChomozygous116673201
8118178403118178404AG17GENIChomozygous116673209
8118179554118179555GA21GENIChomozygous116673211
8118179605118179606AC23GENIChomozygous116673213
8118179766118179767GA23GENIChomozygous116673215
8118181220118181221GA17GENIChomozygous117059803
8118181465118181466CT22GENIChomozygous117059805
8118182231118182232CT13GENIChomozygous116673217
8118186299118186300GT17GENIChomozygous116673221
8118186621118186622GA15GENIChomozygous117059807
8118190683118190684TC26GENIChomozygous116673225
8118190891118190892AG29GENIChomozygous116673227
8118190968118190969CG24GENIChomozygous116673229
8118191706118191707CG18GENIChomozygous116673231
8118194412118194413AG21GENICpossibly homozygous116673239
8118194428118194429TG22GENIChomozygous117059809