| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22982513-22982956 | Common:3; Rare:154 | ||||
| chr14:23010119-23010235 | Rare:35 | ||||
| chr14:23071185-23071332 | Rare:37 | ||||
| chr14:23095093-23095616 | Common:3; Rare:227 | ||||
| chr14:23302390-23302475 | Rare:28 | ||||
| chr14:23306631-23306899 | Common:1; Rare:58 | ||||
| chr14:23321817-23322056 | Common:2; Rare:66 | ||||
| chr14:23555933-23556364 | Common:4; Rare:105 | ||||
| chr14:23567756-23567893 | Rare:29 | ||||
| chr14:23953615-23953823 | Common:8; Rare:83 | ||||
| chr14:23954116-23954305 | Common:2; Rare:54 | ||||
| chr14:23988762-23988938 | Common:8; Rare:72 | ||||
| chr14:24094000-24094417 | Common:5; Rare:114; Clinvar (benign):1 | ||||
| chr14:24114501-24114874 | Common:1; Rare:93 | ||||
| chr14:24114886-24115397 | Common:3; Rare:140 |