| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74816978-74817211 | Rare:46 | ||||
| chr14:75002710-75002972 | Common:1; Rare:86; Clinvar:2 | ||||
| chr14:75051425-75051501 | Common:1; Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:75069449-75069812 | Common:2; Rare:91 | ||||
| chr14:75126954-75127128 | Rare:63 | ||||
| chr14:75279576-75279948 | Common:1; Rare:68 | ||||
| chr14:75578300-75578711 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr14:75579443-75579552 | Common:1; Rare:33; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:75660789-75661510 | Common:7; Rare:188 | ||||
| chr14:75985668-75985798 | Rare:51; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:76151757-76151982 | Rare:82 | ||||
| chr14:77377045-77377410 | Common:2; Rare:107 | ||||
| chr14:77457542-77457876 | Common:1; Rare:99 | ||||
| chr14:77457966-77458207 | Rare:65 | ||||
| chr14:77616741-77617093 | Common:1; Rare:80; Clinvar (benign):2 |