| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20116952-20117012 | Common:1; Rare:13 | ||||
| chr22:20117179-20117590 | Common:3; Rare:132 | ||||
| chr22:20319918-20320158 | Common:2; Rare:93 | ||||
| chr22:20394065-20394176 | Rare:26 | ||||
| chr22:20495781-20495994 | Common:2; Rare:81 | ||||
| chr22:20583210-20583462 | Common:1; Rare:71 | ||||
| chr22:20858696-20859172 | Common:9; Rare:232; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20982190-20982325 | Common:2; Rare:32; Clinvar (benign):2 | ||||
| chr22:21002055-21002211 | Common:3; Rare:62 | ||||
| chr22:21938214-21938295 | Rare:31 | ||||
| chr22:23750979-23751157 | Common:1; Rare:65 | ||||
| chr22:23767940-23768051 | Rare:30 | ||||
| chr22:23787152-23787186 | Rare:11; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:23894011-23894561 | Common:5; Rare:160 | ||||
| chr22:23894570-23894582 | Rare:8 |