| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24213421-24213607 | Common:1; Rare:61 | ||||
| chr14:24232312-24232707 | Common:8; Rare:93 | ||||
| chr14:24232823-24232970 | Common:1; Rare:35 | ||||
| chr14:24242264-24242413 | Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242562-24242763 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271446-24271609 | Common:1; Rare:46 | ||||
| chr14:24299749-24299890 | Common:1; Rare:46 | ||||
| chr14:24367870-24368186 | Common:2; Rare:55 | ||||
| chr14:24429836-24430089 | Common:2; Rare:54 | ||||
| chr14:24442659-24443038 | Common:5; Rare:121 | ||||
| chr14:30559047-30559226 | Common:2; Rare:69 | ||||
| chr14:30622184-30622391 | Common:1; Rare:98 | ||||
| chr14:31025425-31025654 | Common:2; Rare:52 | ||||
| chr14:31207601-31207906 | Common:2; Rare:104 | ||||
| chr14:31420511-31420763 | Common:3; Rare:79 |