| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207626029-207626285 | Common:2; Rare:58 | ||||
| chr2:207711284-207711687 | Common:1; Rare:120 | ||||
| chr2:207769836-207770267 | Common:1; Rare:130 | ||||
| chr2:208025448-208025656 | Common:3; Rare:53 | ||||
| chr2:208254395-208254553 | Common:1; Rare:35 | ||||
| chr2:208255024-208255291 | Common:2; Rare:74 | ||||
| chr2:208265503-208265871 | Common:1; Rare:65 | ||||
| chr2:208265998-208266434 | Common:9; Rare:145; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:208266473-208266590 | Common:1; Rare:30 | ||||
| chr2:208266767-208267041 | Common:4; Rare:53 | ||||
| chr2:210002395-210002646 | Common:6; Rare:82 | ||||
| chr2:210170701-210171147 | Common:1; Rare:145 | ||||
| chr2:210171372-210171612 | Common:4; Rare:91 | ||||
| chr2:210171623-210171771 | Common:1; Rare:48 | ||||
| chr2:210476623-210476915 | Common:4; Rare:80 |