| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30607105-30607315 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:31081139-31081380 | Common:2; Rare:62 | ||||
| chr22:31082979-31083214 | Common:1; Rare:53 | ||||
| chr22:31093160-31093380 | Common:1; Rare:45 | ||||
| chr22:31107417-31107666 | Common:2; Rare:80 | ||||
| chr22:31160092-31160277 | Common:1; Rare:66 | ||||
| chr22:31259141-31259467 | Common:1; Rare:63 | ||||
| chr22:31290667-31290937 | Rare:115 | ||||
| chr22:31292389-31292603 | Common:1; Rare:48 | ||||
| chr22:31399452-31399692 | Rare:70 | ||||
| chr22:31455309-31455492 | Common:2; Rare:49 | ||||
| chr22:31489732-31490158 | Common:3; Rare:171 | ||||
| chr22:31496409-31496602 | Common:2; Rare:56 | ||||
| chr22:31630795-31630846 | Common:1; Rare:15 | ||||
| chr22:31750021-31750297 | Common:3; Rare:80 |