| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20582885-20583183 | Rare:91 | ||||
| chr22:20734071-20734426 | Rare:103 | ||||
| chr22:20858696-20859130 | Common:9; Rare:215; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20917286-20917484 | Rare:74 | ||||
| chr22:20981924-20981990 | Rare:21 | ||||
| chr22:20982185-20982353 | Common:2; Rare:41; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002227 | Common:3; Rare:52 | ||||
| chr22:21629989-21630056 | Common:1; Rare:38 | ||||
| chr22:21642068-21642348 | Common:2; Rare:85 | ||||
| chr22:21694488-21694814 | Common:1; Rare:117 | ||||
| chr22:21938078-21938347 | Rare:84 | ||||
| chr22:23145177-23145532 | Common:3; Rare:120 | ||||
| chr22:23750836-23751227 | Common:4; Rare:113 | ||||
| chr22:23754413-23754605 | Common:4; Rare:43 | ||||
| chr22:23767901-23768037 | Rare:38 |