| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37562477-37562797 | Common:2; Rare:73 | ||||
| chr22:37747444-37747686 | Common:1; Rare:51 | ||||
| chr22:37769021-37769372 | Common:1; Rare:140; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:37772868-37773226 | Common:3; Rare:84 | ||||
| chr22:37773683-37773896 | Rare:50 | ||||
| chr22:37805932-37806436 | Common:4; Rare:133 | ||||
| chr22:37806438-37806516 | Rare:16 | ||||
| chr22:37807060-37807292 | Common:1; Rare:46 | ||||
| chr22:37807362-37807387 | Rare:3 | ||||
| chr22:37863129-37863346 | Rare:51 | ||||
| chr22:37956536-37956834 | Rare:76 | ||||
| chr22:38176148-38176231 | Rare:14 | ||||
| chr22:38204416-38204613 | Common:4; Rare:31 | ||||
| chr22:38228803-38229038 | Common:2; Rare:25 | ||||
| chr22:38295277-38295425 | Common:1; Rare:41 |