| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135984881-135985164 | Common:1; Rare:64 | ||||
| chr2:135985407-135985704 | Common:4; Rare:127; Clinvar (benign):1 | ||||
| chr2:135985854-135985970 | Common:1; Rare:27 | ||||
| chr2:136116160-136116375 | Rare:41 | ||||
| chr2:136118045-136118332 | Rare:79 | ||||
| chr2:137964095-137964310 | Rare:30 | ||||
| chr2:138501639-138502026 | Common:4; Rare:144 | ||||
| chr2:142877540-142877694 | Common:1; Rare:20 | ||||
| chr2:143129041-143129455 | Common:2; Rare:87 | ||||
| chr2:144332443-144332693 | Rare:100 | ||||
| chr2:144513791-144513955 | Rare:44 | ||||
| chr2:144514702-144514931 | Common:1; Rare:40 | ||||
| chr2:144517287-144517699 | Common:6; Rare:122; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144517720-144517755 | Rare:9 | ||||
| chr2:144517764-144517791 | Common:1; Rare:2 |