| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24242580-24242741 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271485-24271613 | Common:1; Rare:36 | ||||
| chr14:24291615-24291876 | Rare:50 | ||||
| chr14:24299664-24299879 | Common:4; Rare:60 | ||||
| chr14:24310011-24310058 | Rare:7 | ||||
| chr14:24429861-24429990 | Common:1; Rare:31 | ||||
| chr14:24442650-24442990 | Common:5; Rare:114 | ||||
| chr14:24819154-24819467 | Common:2; Rare:74 | ||||
| chr14:25049901-25050208 | Common:2; Rare:96 | ||||
| chr14:30559041-30559193 | Common:2; Rare:56 | ||||
| chr14:30622223-30622410 | Common:1; Rare:95 | ||||
| chr14:31025485-31025659 | Common:2; Rare:37 | ||||
| chr14:31121443-31121755 | Common:2; Rare:71 | ||||
| chr14:31207107-31207393 | Rare:81 | ||||
| chr14:31207404-31207911 | Common:2; Rare:158 |