| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24367878-24368213 | Common:2; Rare:57 | ||||
| chr14:24398779-24399291 | Common:5; Rare:145 | ||||
| chr14:24429666-24429974 | Common:2; Rare:80 | ||||
| chr14:24430117-24430305 | Common:3; Rare:57 | ||||
| chr14:24442650-24443023 | Common:5; Rare:120 | ||||
| chr14:25049901-25050209 | Common:2; Rare:96 | ||||
| chr14:30559055-30559187 | Common:2; Rare:45 | ||||
| chr14:30622218-30622365 | Common:1; Rare:70 | ||||
| chr14:31025444-31025653 | Common:2; Rare:47 | ||||
| chr14:31207590-31207883 | Common:2; Rare:103 | ||||
| chr14:31420524-31420741 | Common:3; Rare:66 | ||||
| chr14:31561089-31561539 | Common:4; Rare:126; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:32076185-32076286 | Rare:26 | ||||
| chr14:32076636-32077047 | Common:3; Rare:120 | ||||
| chr14:34462214-34462577 | Common:1; Rare:127 |