chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135734991135734992TG24GENIChomozygous56939133
4135735084135735085AG25GENIChomozygous56939134
4135735246135735247AC17GENIChomozygous56939135
4135735588135735589AG18GENIChomozygous56939136
4135735718135735719AC18GENIChomozygous56939137
4135735729135735730TG19GENIChomozygous56939138
4135735735135735736T-15GENIChomozygous56939139
4135736298135736299CT22GENIChomozygous56939140
4135736667135736668GGTTCA30GENIChomozygous56939141
4135737462135737463AG22GENIChomozygous56939142
4135737827135737828A-11GENIChomozygous56939143
4135737829135737830GA11GENIChomozygous58338661
4135739096135739097AG25GENIChomozygous56939144
4135739431135739432AG28GENIChomozygous56939145
4135739527135739528TC20GENIChomozygous56939146
4135740048135740049AG19GENIChomozygous56939147
4135742352135742353AG20GENIChomozygous56939148
4135742432135742433GGT14GENICheterozygous57338515
4135742719135742720GT21GENIChomozygous56939149
4135742823135742824TC23GENIChomozygous56939150
4135742945135742946TC27GENIChomozygous56939151
4135745185135745197AGCTCCTACTAA------------16GENIChomozygous56939152
4135745668135745669CT13GENIChomozygous56939153
4135746059135746060GGA22GENIChomozygous56939154
4135749126135749127GA24GENIChomozygous56939155
4135749448135749449AG26GENIChomozygous56939156
4135749604135749605GT24GENICpossibly homozygous56939157
4135752014135752015CT17GENIChomozygous56939159
4135752494135752495CA19GENIChomozygous56939160
4135754695135754696CT37GENIChomozygous56939161