chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2127687303127687304CG6GENIChomozygous966081045
2127687717127687718TC14GENIChomozygous966081046
2127688184127688185TC34GENIChomozygous966081047
2127688367127688368GC26GENIChomozygous966081048
2127689696127689697AG19GENIChomozygous966081049
2127690819127690820AG17GENIChomozygous966081050
2127691546127691547AG32GENIChomozygous966081051
2127691651127691652CT19GENIChomozygous966081052
2127693426127693427TG41GENIChomozygous966081053
2127695088127695089CG33GENIChomozygous966081054
2127698127127698128CT8GENIChomozygous966081055
2127698645127698646GC12GENIChomozygous966081056
2127699869127699870GA19GENIChomozygous966081057
2127701576127701577GA40GENIChomozygous966081058
2127702177127702178TC17GENIChomozygous966081059
2127702495127702496AG29GENICpossibly homozygous966081060
2127702652127702653AC24GENIChomozygous966081061
2127703161127703162CT19GENIChomozygous966081062
2127703817127703818AG28GENIChomozygous966081063