| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3379590-3379761 | Common:1; Rare:67 | ||||
| chr2:3519523-3519667 | Common:1; Rare:36 | ||||
| chr2:3558275-3558571 | Common:6; Rare:106 | ||||
| chr2:3575120-3575447 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423379-9423691 | Rare:93 | ||||
| chr2:9474498-9474581 | Common:6; Rare:46 | ||||
| chr2:9555699-9556052 | Common:2; Rare:121 | ||||
| chr2:9843423-9843533 | Common:3; Rare:31 | ||||
| chr2:10689934-10690047 | Common:4; Rare:36 | ||||
| chr2:10812704-10813039 | Common:5; Rare:125 | ||||
| chr2:11746548-11746655 | Common:1; Rare:36; Clinvar:2 | ||||
| chr2:12716604-12717027 | Common:4; Rare:134 | ||||
| chr2:15561300-15561423 | Rare:50 | ||||
| chr2:17753689-17754168 | Common:5; Rare:148; Clinvar (benign):1 | ||||
| chr2:19901944-19902025 | Common:1; Rare:23 |