| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113208641-113208762 | Rare:64 | ||||
| chr13:113490685-113491007 | Common:1; Rare:117 | ||||
| chr13:114281438-114281657 | Common:3; Rare:102 | ||||
| chr13:114281808-114282061 | Common:6; Rare:129 | ||||
| chr14:20343161-20343652 | Common:13; Rare:284 | ||||
| chr14:20455078-20455287 | Common:2; Rare:67 | ||||
| chr14:20683889-20684244 | Common:19; Rare:162; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20684429-20684682 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20999108-20999308 | Rare:44 | ||||
| chr14:21025021-21025191 | Rare:61 | ||||
| chr14:21383932-21384081 | Common:1; Rare:55 | ||||
| chr14:21456056-21456134 | Common:1; Rare:22 | ||||
| chr14:21476878-21477267 | Common:2; Rare:124 | ||||
| chr14:22598138-22598301 | Common:1; Rare:53 | ||||
| chr14:22766549-22766700 | Common:1; Rare:80 |