| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135531834-135532087 | Common:2; Rare:79 | ||||
| chr2:135586312-135586390 | Rare:17 | ||||
| chr2:135741452-135742180 | Common:6; Rare:231 | ||||
| chr2:135742608-135742692 | Rare:20 | ||||
| chr2:135876106-135876231 | Common:2; Rare:33 | ||||
| chr2:135876314-135876681 | Common:1; Rare:107 | ||||
| chr2:135984737-135985293 | Common:1; Rare:128 | ||||
| chr2:135985464-135985740 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr2:135985820-135985958 | Common:1; Rare:28 | ||||
| chr2:136116321-136116590 | Common:3; Rare:42 | ||||
| chr2:136117961-136118326 | Rare:96 | ||||
| chr2:138501585-138501817 | Common:3; Rare:98 | ||||
| chr2:138502091-138502246 | Rare:33 | ||||
| chr2:142877487-142877724 | Common:2; Rare:34 | ||||
| chr2:143128676-143128858 | Common:1; Rare:42 |