| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26345825-26346193 | Common:1; Rare:109 | ||||
| chr2:26764193-26764415 | Common:3; Rare:75 | ||||
| chr2:27032852-27033004 | Rare:61 | ||||
| chr2:27118891-27119177 | Rare:69 | ||||
| chr2:27132024-27132324 | Common:1; Rare:76 | ||||
| chr2:27211695-27212103 | Common:3; Rare:133 | ||||
| chr2:27212225-27212484 | Common:2; Rare:127 | ||||
| chr2:27217296-27217481 | Rare:81 | ||||
| chr2:27323007-27323136 | Rare:37; Clinvar (benign):1 | ||||
| chr2:27356183-27356286 | Rare:24 | ||||
| chr2:27356750-27357193 | Common:2; Rare:133 | ||||
| chr2:27370273-27370690 | Common:2; Rare:170 | ||||
| chr2:27380522-27380894 | Common:2; Rare:136; Clinvar:7 | ||||
| chr2:27442215-27442417 | Common:1; Rare:70 | ||||
| chr2:27495192-27495373 | Rare:58 |