| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:134254031-134254190 | Rare:27 | ||||
| chr2:134918585-134918894 | Common:1; Rare:129 | ||||
| chr2:135052164-135052306 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr2:135531172-135531508 | Common:1; Rare:70 | ||||
| chr2:135742635-135742709 | Rare:22 | ||||
| chr2:135985404-135985451 | Rare:17 | ||||
| chr2:136116163-136116403 | Rare:48 | ||||
| chr2:136116521-136116575 | Common:2; Rare:9 | ||||
| chr2:136117858-136118390 | Rare:143 | ||||
| chr2:138501663-138501903 | Common:1; Rare:97 | ||||
| chr2:142877531-142877684 | Common:1; Rare:20 | ||||
| chr2:148020642-148021098 | Common:2; Rare:104; Clinvar (benign):2 | ||||
| chr2:148021547-148021679 | Rare:26; Clinvar (benign):1 | ||||
| chr2:151828405-151828627 | Common:3; Rare:66 | ||||
| chr2:152717845-152717966 | Rare:50 |