chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135734991135734992TG28GENIChomozygous56939133
4135735084135735085AG28GENIChomozygous56939134
4135735246135735247AC23GENIChomozygous56939135
4135735588135735589AG24GENIChomozygous56939136
4135735718135735719AC18GENIChomozygous56939137
4135735729135735730TG19GENIChomozygous56939138
4135735735135735736T-16GENIChomozygous56939139
4135736298135736299CT11GENIChomozygous56939140
4135736667135736668GGTTCA16GENIChomozygous56939141
4135737462135737463AG26GENIChomozygous56939142
4135737827135737828A-16GENIChomozygous56939143
4135739096135739097AG19GENIChomozygous56939144
4135739431135739432AG29GENIChomozygous56939145
4135739527135739528TC37GENIChomozygous56939146
4135740048135740049AG24GENIChomozygous56939147
4135742352135742353AG11GENIChomozygous56939148
4135742719135742720GT20GENIChomozygous56939149
4135742823135742824TC22GENIChomozygous56939150
4135742945135742946TC29GENIChomozygous56939151
4135745185135745197AGCTCCTACTAA------------14GENIChomozygous56939152
4135745668135745669CT16GENIChomozygous56939153
4135746059135746060GGA12GENIChomozygous56939154
4135749126135749127GA21GENIChomozygous56939155
4135749448135749449AG15GENIChomozygous56939156
4135749604135749605GT19GENIChomozygous56939157
4135751572135751574AT--4GENIChomozygous56939158
4135752014135752015CT17GENIChomozygous56939159
4135752494135752495CA17GENIChomozygous56939160
4135754695135754696CT23GENIChomozygous56939161
4135758406135758407AATG8GENIChomozygous56939163