chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119113567491135675GA23GENIChomozygous50865134
119113579191135792AG30GENIChomozygous50865135
119113927791139278GA31GENIChomozygous50865136
119113946391139464GT33GENICpossibly homozygous50865137
119113990291139903CCT13GENICheterozygous50865138
119114100091141001CCAGATAGCTACTGCTA7GENIChomozygous50865139
119114130191141302GA27GENIChomozygous50865141
119114184391141844TA16GENIChomozygous50865142
119114259991142600GC9GENIChomozygous50865143
119114319991143200CT31GENIChomozygous50865144
119114378791143788CA28GENIChomozygous50865145
119114413091144136ACCACC------25GENIChomozygous50865146
119114413591144136CCA32GENICheterozygous50865147
119114439091144391AG29GENIChomozygous50865148
119114510391145104TG6GENIChomozygous50865149
119114511791145118GGTGCGC1GENIChomozygous50865150
119114526891145269GGA8GENICheterozygous50865151
119114527691145277TA10GENIChomozygous50865152
119114550291145503CT23GENIChomozygous50865153
119114623491146235C-14GENIChomozygous50865154
119114623991146242AAA---6GENICheterozygous50865155
119114624091146242AA--6GENICheterozygous50865156
119114628691146287CA19GENIChomozygous50865157
119114629091146291AC18GENICpossibly homozygous50865158