| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217901914-217902175 | Common:3; Rare:42 | ||||
| chr2:217905434-217905614 | Rare:36 | ||||
| chr2:217978770-217978941 | Common:1; Rare:50 | ||||
| chr2:218129107-218129327 | Rare:35 | ||||
| chr2:218217049-218217247 | Common:1; Rare:70 | ||||
| chr2:218269998-218270590 | Common:6; Rare:190; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218279029-218279356 | Common:2; Rare:93 | ||||
| chr2:218287265-218287411 | Rare:24 | ||||
| chr2:218292455-218292646 | Common:1; Rare:54 | ||||
| chr2:218381922-218382234 | Common:2; Rare:57 | ||||
| chr2:218398573-218398751 | Common:2; Rare:65 | ||||
| chr2:218399494-218399684 | Common:1; Rare:80 | ||||
| chr2:218568276-218568665 | Common:3; Rare:102 | ||||
| chr2:218568781-218568972 | Common:1; Rare:59 | ||||
| chr2:218659338-218659382 | Common:1; Rare:10 |