| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20319960-20320160 | Common:2; Rare:76 | ||||
| chr22:20394013-20394194 | Rare:57 | ||||
| chr22:20495781-20495999 | Common:2; Rare:82 | ||||
| chr22:20582940-20583152 | Rare:62 | ||||
| chr22:20858699-20859150 | Common:9; Rare:222; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20917119-20917484 | Rare:128 | ||||
| chr22:20982201-20982353 | Common:2; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002215 | Common:3; Rare:49 | ||||
| chr22:21629989-21630060 | Common:1; Rare:40 | ||||
| chr22:21642044-21642348 | Common:2; Rare:92 | ||||
| chr22:21694559-21694812 | Common:1; Rare:87 | ||||
| chr22:21867406-21867752 | Common:4; Rare:97 | ||||
| chr22:21938261-21938311 | Rare:23 | ||||
| chr22:22887701-22887890 | Common:7; Rare:47 | ||||
| chr22:23750937-23751220 | Common:4; Rare:91 |