| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30356864-30357010 | Common:1; Rare:49 | ||||
| chr22:30607045-30607209 | Common:3; Rare:47; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:31292462-31292590 | Rare:26 | ||||
| chr22:31399444-31399633 | Rare:47 | ||||
| chr22:31489803-31489917 | Rare:43 | ||||
| chr22:31496046-31496198 | Common:1; Rare:39 | ||||
| chr22:31496421-31496563 | Common:1; Rare:36 | ||||
| chr22:31662209-31662364 | Common:2; Rare:61 | ||||
| chr22:31753791-31753987 | Rare:70 | ||||
| chr22:31944325-31944680 | Common:5; Rare:150 | ||||
| chr22:32412188-32412305 | Common:1; Rare:38 | ||||
| chr22:32475169-32475337 | Common:2; Rare:47 | ||||
| chr22:35299566-35299902 | Common:3; Rare:80 | ||||
| chr22:35399896-35400207 | Rare:110 | ||||
| chr22:35648279-35648476 | Common:2; Rare:33 |