chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221236959221236960TG15GENIChomozygous108544055
1221237018221237019GA14GENIChomozygous108544057
1221237848221237849AG6GENIChomozygous108544059
1221238196221238197AG14GENIChomozygous108544061
1221238310221238311CT9GENIChomozygous108544063
1221238905221238906CT12GENIChomozygous108544067
1221239053221239054AG14GENIChomozygous108544069
1221239057221239058AG13GENIChomozygous108544071
1221239488221239489TC18GENIChomozygous108544073
1221239984221239985CT15GENIChomozygous108994668
1221241147221241148AG13GENIChomozygous108544075
1221241468221241469AG12GENIChomozygous108544077
1221241562221241563GA13GENIChomozygous108544079
1221241592221241593TG13GENIChomozygous108544081
1221241931221241932CT13GENIChomozygous108544083
1221242777221242778GA10GENIChomozygous108544085
1221243079221243080AG16GENIChomozygous108544087
1221243705221243706GA20GENIChomozygous108544089
1221243875221243876TA16GENIChomozygous108544091
1221243971221243972TA12GENIChomozygous108544093
1221242965221242968AGG14GENIChomozygous127485728