| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20079930-20080299 | Common:1; Rare:123 | ||||
| chr22:20116951-20117022 | Common:1; Rare:19 | ||||
| chr22:20117135-20117652 | Common:4; Rare:167 | ||||
| chr22:20319998-20320158 | Common:1; Rare:53 | ||||
| chr22:20495781-20495956 | Common:2; Rare:68 | ||||
| chr22:20507496-20507636 | Rare:36 | ||||
| chr22:20917162-20917418 | Rare:89 | ||||
| chr22:20982196-20982358 | Common:2; Rare:37; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002061-21002272 | Common:5; Rare:82 | ||||
| chr22:21629954-21630286 | Common:3; Rare:109 | ||||
| chr22:21642025-21642364 | Common:2; Rare:105 | ||||
| chr22:21665934-21666102 | Common:1; Rare:53 | ||||
| chr22:22508717-22508908 | Rare:58 | ||||
| chr22:22520270-22520475 | Common:6; Rare:42 | ||||
| chr22:22558991-22559364 | Common:1; Rare:118 |