| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135741611-135742213 | Common:4; Rare:203 | ||||
| chr2:135914392-135914494 | Rare:21; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:138501623-138501951 | Common:4; Rare:128 | ||||
| chr2:142877511-142877837 | Common:2; Rare:54 | ||||
| chr2:148020645-148021153 | Common:2; Rare:125; Clinvar (benign):2 | ||||
| chr2:148021497-148021679 | Rare:41; Clinvar (benign):1 | ||||
| chr2:149587211-149587365 | Common:1; Rare:33 | ||||
| chr2:149587666-149587903 | Common:1; Rare:72; Clinvar:2 | ||||
| chr2:150487186-150487315 | Rare:29 | ||||
| chr2:151828329-151828619 | Common:3; Rare:89 | ||||
| chr2:152175604-152176060 | Common:2; Rare:134 | ||||
| chr2:152335423-152335590 | Rare:61 | ||||
| chr2:152658984-152659191 | Rare:62 | ||||
| chr2:152717135-152717259 | Rare:49 | ||||
| chr2:156332653-156332904 | Rare:79; Clinvar:3 |