| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27086532-27086797 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr2:27211722-27212065 | Common:3; Rare:117 | ||||
| chr2:27212225-27212387 | Common:2; Rare:87 | ||||
| chr2:27217296-27217504 | Rare:85 | ||||
| chr2:27323063-27323154 | Rare:21 | ||||
| chr2:27356737-27357150 | Common:1; Rare:120 | ||||
| chr2:27370257-27370641 | Common:1; Rare:158 | ||||
| chr2:27489647-27489958 | Rare:81; Clinvar (benign):1 | ||||
| chr2:27582961-27583128 | Rare:61 | ||||
| chr2:27628954-27629127 | Common:1; Rare:95 | ||||
| chr2:27663351-27663434 | Rare:24 | ||||
| chr2:27663518-27663926 | Rare:143 | ||||
| chr2:27771649-27772005 | Common:1; Rare:112 | ||||
| chr2:27890454-27890825 | Rare:95 | ||||
| chr2:28566424-28566512 | Rare:25 |