| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27086270-27086362 | Rare:18 | ||||
| chr2:27086480-27086832 | Common:6; Rare:107; Clinvar (benign):3 | ||||
| chr2:27087106-27087252 | Rare:33; Clinvar:2 | ||||
| chr2:27118473-27118755 | Rare:67 | ||||
| chr2:27123730-27123870 | Common:2; Rare:32 | ||||
| chr2:27134559-27134896 | Common:1; Rare:132 | ||||
| chr2:27202976-27203224 | Rare:45 | ||||
| chr2:27211210-27211426 | Rare:46 | ||||
| chr2:27211585-27211793 | Rare:51 | ||||
| chr2:27211870-27212452 | Common:6; Rare:251 | ||||
| chr2:27212771-27212837 | Rare:11 | ||||
| chr2:27212956-27213065 | Rare:33 | ||||
| chr2:27213248-27213309 | Rare:21 | ||||
| chr2:27217214-27217829 | Common:1; Rare:208 | ||||
| chr2:27217838-27218207 | Common:5; Rare:122; Clinvar (pathogenic):1 |