| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150407922-150408372 | Common:2; Rare:132 | ||||
| chr3:150408832-150408997 | Rare:48 | ||||
| chr3:150545427-150546507 | Common:16; Rare:442 | ||||
| chr3:150603129-150603387 | Common:4; Rare:191 | ||||
| chr3:150703720-150704220 | Common:6; Rare:282 | ||||
| chr3:150763001-150763309 | Common:2; Rare:145 | ||||
| chr3:150763322-150763618 | Common:2; Rare:134 | ||||
| chr3:152268566-152268999 | Common:4; Rare:329 | ||||
| chr3:153162043-153162240 | Rare:63 | ||||
| chr3:154121295-154121479 | Common:6; Rare:158 | ||||
| chr3:155745017-155745169 | Rare:72 | ||||
| chr3:155854305-155854839 | Common:2; Rare:277; Clinvar (benign):2 | ||||
| chr3:155870314-155870768 | Common:4; Rare:247 | ||||
| chr3:156555059-156555326 | Common:2; Rare:214 | ||||
| chr3:156674326-156674651 | Common:8; Rare:178 |