Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48645903-48646460 | Common:1; Rare:103 | ||||
chr19:48810852-48811127 | Rare:86 | ||||
chr19:48872210-48872471 | Common:2; Rare:94 | ||||
chr19:48933597-48933696 | Common:3; Rare:26 | ||||
chr19:48954735-48954974 | Rare:84 | ||||
chr19:48965196-48965458 | Rare:74; Clinvar:1; Clinvar (pathogenic):5 | ||||
chr19:48965627-48965850 | Common:1; Rare:86; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr19:48993247-48993579 | Common:3; Rare:146; Clinvar:3; Clinvar (benign):2 | ||||
chr19:48993738-48993913 | Common:5; Rare:54 | ||||
chr19:49085084-49085535 | Common:3; Rare:174 | ||||
chr19:49085654-49085981 | Common:1; Rare:107 | ||||
chr19:49114129-49114405 | Common:4; Rare:67 | ||||
chr19:49115003-49115089 | Common:1; Rare:23 | ||||
chr19:49118752-49118904 | Rare:64 | ||||
chr19:49142977-49143139 | Common:4; Rare:41 |