| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38192080-38192222 | Common:2; Rare:23 | ||||
| chr22:38201810-38202155 | Common:2; Rare:95 | ||||
| chr22:38300831-38301198 | Common:2; Rare:92 | ||||
| chr22:38398817-38399213 | Common:5; Rare:172 | ||||
| chr22:38505950-38506016 | Rare:18 | ||||
| chr22:38506254-38506630 | Common:1; Rare:125 | ||||
| chr22:38570184-38570522 | Common:6; Rare:65 | ||||
| chr22:38656340-38656706 | Common:1; Rare:98 | ||||
| chr22:38681821-38682041 | Common:2; Rare:93 | ||||
| chr22:38725994-38726341 | Common:1; Rare:86 | ||||
| chr22:38739401-38739549 | Common:2; Rare:34 | ||||
| chr22:38739743-38740134 | Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:38742525-38742661 | Common:1; Rare:46 | ||||
| chr22:38754466-38754678 | Common:1; Rare:44 | ||||
| chr22:38755387-38755598 | Common:1; Rare:39 |