chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221236959221236960TG18GENIChomozygous108544055
1221237018221237019GA24GENIChomozygous108544057
1221237848221237849AG21GENICpossibly homozygous108544059
1221238196221238197AG19GENIChomozygous108544061
1221238310221238311CT16GENIChomozygous108544063
1221238905221238906CT20GENIChomozygous108544067
1221239053221239054AG28GENIChomozygous108544069
1221239057221239058AG28GENIChomozygous108544071
1221239488221239489TC23GENIChomozygous108544073
1221239984221239985CT26GENIChomozygous108994668
1221241147221241148AG20GENIChomozygous108544075
1221241468221241469AG24GENIChomozygous108544077
1221241562221241563GA20GENIChomozygous108544079
1221241592221241593TG21GENIChomozygous108544081
1221241931221241932CT30GENIChomozygous108544083
1221242777221242778GA21GENIChomozygous108544085
1221243079221243080AG19GENIChomozygous108544087
1221243705221243706GA20GENIChomozygous108544089
1221243875221243876TA23GENIChomozygous108544091
1221243971221243972TA25GENIChomozygous108544093
1221242965221242968AGG15GENIChomozygous127485728