| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27211747-27212103 | Common:3; Rare:122 | ||||
| chr2:27212225-27212467 | Common:2; Rare:124 | ||||
| chr2:27217115-27217554 | Common:1; Rare:153 | ||||
| chr2:27263038-27263302 | Common:1; Rare:57 | ||||
| chr2:27282331-27282526 | Rare:30 | ||||
| chr2:27323007-27323150 | Rare:42; Clinvar (benign):1 | ||||
| chr2:27356743-27357195 | Common:2; Rare:137 | ||||
| chr2:27370254-27370648 | Common:1; Rare:160 | ||||
| chr2:27489662-27489955 | Rare:74; Clinvar (benign):1 | ||||
| chr2:27582997-27583106 | Rare:41 | ||||
| chr2:27628949-27629073 | Common:1; Rare:59 | ||||
| chr2:27663351-27663498 | Rare:37 | ||||
| chr2:27663513-27663931 | Rare:146 | ||||
| chr2:27771548-27772068 | Common:1; Rare:156 | ||||
| chr2:27772125-27772533 | Common:1; Rare:74 |