chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221236959221236960TG22GENIChomozygous108544055
1221237018221237019GA20GENIChomozygous108544057
1221237848221237849AG14GENIChomozygous108544059
1221238196221238197AG24GENICpossibly homozygous108544061
1221238310221238311CT17GENIChomozygous108544063
1221238905221238906CT21GENIChomozygous108544067
1221239053221239054AG23GENIChomozygous108544069
1221239057221239058AG23GENIChomozygous108544071
1221239488221239489TC19GENIChomozygous108544073
1221239984221239985CT20GENIChomozygous108994668
1221241147221241148AG16GENIChomozygous108544075
1221241468221241469AG17GENIChomozygous108544077
1221241562221241563GA18GENICpossibly homozygous108544079
1221241592221241593TG19GENIChomozygous108544081
1221241931221241932CT21GENIChomozygous108544083
1221242777221242778GA33GENIChomozygous108544085
1221243079221243080AG26GENIChomozygous108544087
1221243705221243706GA21GENIChomozygous108544089
1221243875221243876TA25GENIChomozygous108544091
1221243971221243972TA32GENIChomozygous108544093