| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27051196-27051252 | Common:3; Rare:54 | ||||
| chr2:27051466-27051687 | Rare:65 | ||||
| chr2:27071579-27071901 | Common:1; Rare:100 | ||||
| chr2:27072080-27072255 | Rare:24 | ||||
| chr2:27086443-27086836 | Common:6; Rare:116; Clinvar (benign):3 | ||||
| chr2:27123723-27123926 | Common:2; Rare:53 | ||||
| chr2:27134546-27134758 | Common:1; Rare:93 | ||||
| chr2:27211255-27211435 | Rare:40 | ||||
| chr2:27211895-27212125 | Common:3; Rare:82 | ||||
| chr2:27212185-27212623 | Common:3; Rare:177 | ||||
| chr2:27212741-27212976 | Rare:45 | ||||
| chr2:27217244-27217603 | Rare:143 | ||||
| chr2:27322962-27323248 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr2:27356142-27356314 | Common:1; Rare:40 | ||||
| chr2:27356344-27356606 | Common:1; Rare:101 |