| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74147857-74148052 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178792-74179066 | Common:4; Rare:84 | ||||
| chr2:74198424-74198637 | Rare:82 | ||||
| chr2:74421567-74421781 | Rare:72 | ||||
| chr2:74454828-74455138 | Rare:83 | ||||
| chr2:74458143-74458504 | Common:1; Rare:110 | ||||
| chr2:74459691-74459954 | Rare:91 | ||||
| chr2:74465335-74465446 | Rare:31; Clinvar:1 | ||||
| chr2:74472347-74472758 | Common:4; Rare:188 | ||||
| chr2:74482894-74483130 | Common:1; Rare:86 | ||||
| chr2:74503024-74503150 | Rare:28 | ||||
| chr2:74503307-74503454 | Rare:36 | ||||
| chr2:74507343-74507519 | Rare:50 | ||||
| chr2:74507639-74507779 | Rare:35 | ||||
| chr2:74527480-74527744 | Common:1; Rare:91 |