| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24094138-24094519 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr14:24094870-24095426 | Common:3; Rare:125 | ||||
| chr14:24095571-24095724 | Common:1; Rare:33 | ||||
| chr14:24102691-24102976 | Common:1; Rare:87 | ||||
| chr14:24103102-24103240 | Rare:53; Clinvar:4 | ||||
| chr14:24113835-24114108 | Common:2; Rare:69 | ||||
| chr14:24114938-24115358 | Common:2; Rare:119 | ||||
| chr14:24141577-24141862 | Common:1; Rare:61 | ||||
| chr14:24146551-24146673 | Rare:50 | ||||
| chr14:24147243-24147501 | Common:2; Rare:70 | ||||
| chr14:24165878-24166156 | Common:1; Rare:73 | ||||
| chr14:24195391-24195791 | Common:2; Rare:99 | ||||
| chr14:24213408-24213539 | Rare:48 | ||||
| chr14:24232285-24232929 | Common:9; Rare:157 | ||||
| chr14:24242293-24242433 | Rare:46; Clinvar (benign):1 |