| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70293619-70293841 | Common:2; Rare:74 | ||||
| chr2:71068040-71068328 | Rare:76 | ||||
| chr2:71068526-71068678 | Rare:73 | ||||
| chr2:71130194-71130662 | Common:6; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071701-73071848 | Common:2; Rare:57 | ||||
| chr2:73214146-73214305 | Common:1; Rare:59 | ||||
| chr2:73233200-73233495 | Common:1; Rare:84 | ||||
| chr2:73234195-73234361 | Common:2; Rare:50 | ||||
| chr2:73828873-73829005 | Rare:32 | ||||
| chr2:74147862-74148052 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178779-74179066 | Common:4; Rare:85 | ||||
| chr2:74198389-74198637 | Rare:89 | ||||
| chr2:74391793-74392202 | Common:2; Rare:177 | ||||
| chr2:74421582-74421781 | Rare:69 | ||||
| chr2:74465350-74465455 | Common:1; Rare:29; Clinvar:1 |