| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27322991-27323176 | Common:2; Rare:106; Clinvar (benign):2 | ||||
| chr2:27356142-27356318 | Common:2; Rare:74 | ||||
| chr2:27356360-27356610 | Common:2; Rare:173 | ||||
| chr2:27356604-27356940 | Common:1; Rare:131 | ||||
| chr2:27356951-27357227 | Common:4; Rare:187 | ||||
| chr2:27370227-27370680 | Common:4; Rare:357 | ||||
| chr2:27409456-27409785 | Rare:213 | ||||
| chr2:27428970-27429230 | Common:2; Rare:139 | ||||
| chr2:27433480-27434030 | Common:4; Rare:144 | ||||
| chr2:27489678-27490013 | Common:1; Rare:85; Clinvar (benign):1 | ||||
| chr2:27495186-27495338 | Rare:53 | ||||
| chr2:27496080-27496637 | Common:1; Rare:132 | ||||
| chr2:27496716-27496916 | Rare:63 | ||||
| chr2:27582785-27583130 | Rare:224 | ||||
| chr2:27628959-27629101 | Common:2; Rare:136 |