| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74147821-74148173 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74178808-74179009 | Common:2; Rare:56 | ||||
| chr2:74198424-74198659 | Rare:101 | ||||
| chr2:74374645-74374803 | Rare:34 | ||||
| chr2:74391784-74392161 | Common:2; Rare:172 | ||||
| chr2:74421556-74421781 | Rare:74 | ||||
| chr2:74440419-74440651 | Rare:61 | ||||
| chr2:74454860-74455138 | Rare:76 | ||||
| chr2:74458095-74458509 | Common:1; Rare:127 | ||||
| chr2:74465367-74465461 | Common:1; Rare:23 | ||||
| chr2:74482902-74483129 | Common:1; Rare:84 | ||||
| chr2:74499562-74499776 | Common:2; Rare:40 | ||||
| chr2:74502968-74503146 | Rare:41 | ||||
| chr2:74507224-74507474 | Common:2; Rare:65 | ||||
| chr2:74507599-74507911 | Common:1; Rare:83 |