| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73950035-73950351 | Common:6; Rare:141; Clinvar (benign):5 | ||||
| chr14:74019233-74019436 | Common:1; Rare:81 | ||||
| chr14:74493279-74493781 | Common:4; Rare:157; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:74713042-74713198 | Rare:89 | ||||
| chr14:75002741-75002947 | Common:1; Rare:59; Clinvar:2 | ||||
| chr14:75127008-75127106 | Rare:26 | ||||
| chr14:75660813-75661373 | Common:5; Rare:140 | ||||
| chr14:76762155-76762219 | Common:1; Rare:15 | ||||
| chr14:77377030-77377421 | Common:3; Rare:115 | ||||
| chr14:77457555-77457844 | Common:1; Rare:89 | ||||
| chr14:77707991-77708114 | Rare:59 | ||||
| chr14:77761112-77761275 | Common:1; Rare:59 | ||||
| chr14:81220867-81221046 | Common:1; Rare:86 | ||||
| chr14:81221279-81221341 | Rare:8 | ||||
| chr14:81436403-81436585 | Common:3; Rare:67 |