| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20319998-20320202 | Common:1; Rare:70 | ||||
| chr22:20495781-20495974 | Common:2; Rare:73 | ||||
| chr22:20507490-20507636 | Rare:39 | ||||
| chr22:20507923-20508074 | Rare:34 | ||||
| chr22:20917185-20917413 | Rare:83 | ||||
| chr22:20982196-20982363 | Common:2; Rare:40; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:21002043-21002250 | Common:4; Rare:79 | ||||
| chr22:21642042-21642348 | Common:2; Rare:94 | ||||
| chr22:23750937-23751159 | Common:3; Rare:78 | ||||
| chr22:23894045-23894509 | Common:5; Rare:137 | ||||
| chr22:23894524-23894915 | Common:3; Rare:161; Clinvar:1 | ||||
| chr22:23974364-23974691 | Common:1; Rare:4 | ||||
| chr22:24011029-24011471 | Common:43; Rare:222 | ||||
| chr22:24270687-24270973 | Common:3; Rare:103 | ||||
| chr22:24555884-24556045 | Rare:51 |