| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130836751-130836922 | Common:2; Rare:65 | ||||
| chr2:131093107-131093566 | Common:2; Rare:177 | ||||
| chr2:131105228-131105393 | Common:2; Rare:79 | ||||
| chr2:131492091-131492219 | Common:2; Rare:39 | ||||
| chr2:131492279-131492441 | Common:3; Rare:69 | ||||
| chr2:131492743-131492970 | Common:5; Rare:73 | ||||
| chr2:131492980-131493143 | Common:3; Rare:45 | ||||
| chr2:132417317-132417327 | Rare:1 | ||||
| chr2:132670116-132670305 | Common:2; Rare:44 | ||||
| chr2:133568215-133568571 | Common:2; Rare:63 | ||||
| chr2:134918589-134919017 | Common:1; Rare:162 | ||||
| chr2:135052196-135052481 | Common:1; Rare:112; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:135531159-135531533 | Common:1; Rare:80 | ||||
| chr2:135741608-135742007 | Common:4; Rare:140 | ||||
| chr2:135911142-135911489 | Common:1; Rare:92; Clinvar (benign):2; Clinvar (pathogenic):2 |