| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20495771-20496002 | Common:2; Rare:83 | ||||
| chr22:20507496-20507633 | Rare:32 | ||||
| chr22:20507938-20508070 | Rare:32 | ||||
| chr22:20858696-20859158 | Common:9; Rare:227; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20917286-20917461 | Rare:70 | ||||
| chr22:20982167-20982353 | Common:2; Rare:51; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002061-21002262 | Common:5; Rare:80 | ||||
| chr22:21629979-21630262 | Common:2; Rare:96 | ||||
| chr22:21642062-21642353 | Common:2; Rare:86 | ||||
| chr22:21665941-21666070 | Rare:39 | ||||
| chr22:21867322-21867757 | Common:4; Rare:116 | ||||
| chr22:21938200-21938345 | Rare:46 | ||||
| chr22:22520256-22520500 | Common:6; Rare:57 | ||||
| chr22:23767925-23768082 | Rare:39 | ||||
| chr22:23857063-23857155 | Common:8; Rare:36 |