| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74493193-74493795 | Common:4; Rare:199; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:74611590-74611660 | Rare:23 | ||||
| chr14:74612174-74612391 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr14:74713026-74713207 | Common:1; Rare:101 | ||||
| chr14:74809971-74810269 | Rare:62 | ||||
| chr14:74881833-74881991 | Rare:74 | ||||
| chr14:75002741-75002972 | Common:1; Rare:72; Clinvar:2 | ||||
| chr14:75063988-75064184 | Common:1; Rare:49 | ||||
| chr14:75069455-75069732 | Common:2; Rare:71 | ||||
| chr14:75126989-75127110 | Rare:39 | ||||
| chr14:75147667-75148049 | Common:3; Rare:61 | ||||
| chr14:75176355-75176517 | Rare:37 | ||||
| chr14:75176525-75176855 | Common:1; Rare:94 | ||||
| chr14:75278776-75279137 | Common:2; Rare:107 | ||||
| chr14:75279485-75279675 | Rare:40 |