| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20079916-20080253 | Common:1; Rare:107 | ||||
| chr22:20117135-20117606 | Common:3; Rare:150 | ||||
| chr22:20319989-20320179 | Common:2; Rare:66 | ||||
| chr22:20393948-20394262 | Common:1; Rare:91 | ||||
| chr22:20495768-20495926 | Common:2; Rare:58 | ||||
| chr22:20507490-20507622 | Rare:31 | ||||
| chr22:20858704-20859066 | Common:5; Rare:175; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:20917100-20917529 | Rare:145 | ||||
| chr22:20982196-20982353 | Common:2; Rare:36; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002052-21002261 | Common:5; Rare:84 | ||||
| chr22:21032551-21032663 | Rare:48 | ||||
| chr22:21642015-21642372 | Common:2; Rare:109 | ||||
| chr22:21651915-21652192 | Common:2; Rare:58 | ||||
| chr22:21665945-21666070 | Rare:36 | ||||
| chr22:21867421-21867739 | Common:3; Rare:92 |