| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24232537-24232721 | Rare:44 | ||||
| chr14:24232823-24232949 | Common:1; Rare:26 | ||||
| chr14:24242276-24242433 | Rare:52; Clinvar (benign):2 | ||||
| chr14:24242538-24242741 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24271453-24271604 | Common:1; Rare:43 | ||||
| chr14:24299701-24299893 | Common:4; Rare:62 | ||||
| chr14:24368043-24368191 | Common:1; Rare:26 | ||||
| chr14:24429855-24429980 | Rare:30 | ||||
| chr14:24442666-24443023 | Common:5; Rare:114 | ||||
| chr14:25049890-25050197 | Common:3; Rare:94 | ||||
| chr14:30559094-30559191 | Common:1; Rare:31 | ||||
| chr14:30622197-30622362 | Common:1; Rare:68 | ||||
| chr14:31025310-31025662 | Common:2; Rare:77 | ||||
| chr14:31026357-31026608 | Common:3; Rare:78 | ||||
| chr14:31207473-31207906 | Common:2; Rare:140 |