| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208265505-208265859 | Common:1; Rare:62 | ||||
| chr2:208265901-208266391 | Common:9; Rare:158; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:208266473-208266623 | Common:2; Rare:38 | ||||
| chr2:209423742-209424048 | Common:2; Rare:92 | ||||
| chr2:210002349-210002646 | Common:6; Rare:89 | ||||
| chr2:210170425-210170496 | Rare:9 | ||||
| chr2:210170685-210171008 | Common:2; Rare:117 | ||||
| chr2:210171060-210171183 | Rare:25 | ||||
| chr2:210171360-210171589 | Common:4; Rare:89 | ||||
| chr2:210476634-210476905 | Common:2; Rare:76 | ||||
| chr2:213150381-213150772 | Common:6; Rare:75 | ||||
| chr2:213151141-213151374 | Rare:31 | ||||
| chr2:213151504-213152394 | Common:8; Rare:277 | ||||
| chr2:213152533-213152600 | Common:1; Rare:12 | ||||
| chr2:213284142-213284504 | Rare:112 |