chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119113567491135675GA22GENIChomozygous50865134
119113579191135792AG27GENIChomozygous50865135
119113927791139278GA25GENIChomozygous50865136
119113946391139464GT29GENIChomozygous50865137
119113990291139903CCT11GENICpossibly homozygous50865138
119114100091141001CCAGATAGCTACTGCTA22GENIChomozygous50865139
119114130191141302GA27GENIChomozygous50865141
119114184391141844TA17GENIChomozygous50865142
119114259991142600GC9GENIChomozygous50865143
119114319991143200CT30GENIChomozygous50865144
119114378791143788CA21GENIChomozygous50865145
119114413091144136ACCACC------35GENIChomozygous50865146
119114439091144391AG29GENIChomozygous50865148
119114510391145104TG7GENIChomozygous50865149
119114510791145110TGT---6GENIChomozygous51261705
119114527691145277TA10GENIChomozygous50865152
119114550291145503CT22GENIChomozygous50865153
119114623491146235C-17GENIChomozygous50865154
119114623591146236TA17GENIChomozygous51193058
119114623991146242AAA---9GENICheterozygous50865155
119114624091146242AA--9GENICheterozygous50865156
119114624191146242A-9GENICheterozygous51230245
119114629091146291AC19GENIChomozygous50865158
119114629591146296AC20GENIChomozygous50898814