| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114281474-114282110 | Common:9; Rare:328 | ||||
| chr13:114282122-114282430 | Common:4; Rare:94 | ||||
| chr14:20332677-20332789 | Rare:20 | ||||
| chr14:20333252-20333416 | Common:1; Rare:33 | ||||
| chr14:20343184-20343669 | Common:12; Rare:291 | ||||
| chr14:20413162-20413224 | Common:1; Rare:9 | ||||
| chr14:20413420-20413595 | Common:3; Rare:50 | ||||
| chr14:20454731-20455305 | Common:7; Rare:152 | ||||
| chr14:20461379-20461638 | Common:1; Rare:82 | ||||
| chr14:20684447-20684629 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr14:20989641-20990011 | Common:8; Rare:84 | ||||
| chr14:21024884-21025235 | Common:1; Rare:121 | ||||
| chr14:21025494-21025566 | Common:1; Rare:17 | ||||
| chr14:21025675-21026064 | Common:2; Rare:67 | ||||
| chr14:21383923-21384264 | Common:8; Rare:114 |