| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20495775-20495994 | Common:2; Rare:82 | ||||
| chr22:20507496-20507624 | Rare:28 | ||||
| chr22:20773795-20774134 | Common:2; Rare:57 | ||||
| chr22:20858968-20859115 | Common:5; Rare:86; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20917275-20917433 | Rare:57 | ||||
| chr22:20982190-20982358 | Common:2; Rare:41; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002092-21002251 | Common:4; Rare:57 | ||||
| chr22:21665893-21666102 | Common:1; Rare:66 | ||||
| chr22:21867619-21867808 | Common:1; Rare:58 | ||||
| chr22:21937955-21938295 | Rare:103 | ||||
| chr22:21952813-21952969 | Common:1; Rare:58 | ||||
| chr22:21982754-21982950 | Rare:48 | ||||
| chr22:23145171-23145551 | Common:3; Rare:124 | ||||
| chr22:23786852-23787038 | Common:1; Rare:71; Clinvar:3 | ||||
| chr22:23856850-23856969 | Common:1; Rare:37 |