chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5133929901133929902GA12GENIChomozygous114015172
5133929918133929919GA12GENIChomozygous118858407
5133929919133929920AG13GENIChomozygous118858408
5133930091133930092CT12GENIChomozygous118983112
5133931771133931772AG16GENIChomozygous114015173
5133932583133932584GA22GENIChomozygous114143374
5133933383133933384TC27GENIChomozygous114143375
5133934338133934339TC23GENIChomozygous114015175
5133945596133945597GA17GENIChomozygous114143378
5133946754133946755AT24GENIChomozygous114143379
5133947140133947141CA30GENICpossibly homozygous114143380
5133947627133947628TC9GENIChomozygous114015180
5133949653133949654AG20GENIChomozygous114015181
5133949654133949655AG19GENIChomozygous114015182
5133950589133950590AG25GENIChomozygous114143381
5133951146133951147AC26GENIChomozygous114015183
5133956027133956028AG12GENIChomozygous114143382