| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37805962-37806163 | Common:1; Rare:64 | ||||
| chr22:37806172-37806561 | Common:4; Rare:73 | ||||
| chr22:37816220-37816624 | Common:2; Rare:114 | ||||
| chr22:40360256-40360486 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:40499807-40499893 | Common:1; Rare:13 | ||||
| chr22:40509943-40510044 | Common:1; Rare:19 | ||||
| chr22:40967668-40967880 | Rare:45 | ||||
| chr22:41256024-41256272 | Common:1; Rare:80 | ||||
| chr22:41413940-41414052 | Rare:37 | ||||
| chr22:41523018-41523274 | Rare:67 | ||||
| chr22:41694941-41694963 | Rare:1 | ||||
| chr22:41695015-41695543 | Common:4; Rare:95 | ||||
| chr22:41697228-41697509 | Common:1; Rare:60 | ||||
| chr22:42159851-42160025 | Common:2; Rare:38 | ||||
| chr22:42369251-42369492 | Common:3; Rare:59 |