| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36296222-36296532 | Common:1; Rare:65 | ||||
| chr22:36301077-36301163 | Common:1; Rare:26 | ||||
| chr22:36310294-36310320 | Rare:6 | ||||
| chr22:36331436-36331760 | Common:4; Rare:55 | ||||
| chr22:36395162-36395300 | Common:1; Rare:21 | ||||
| chr22:37075029-37075184 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:37518064-37518295 | Common:1; Rare:53 | ||||
| chr22:37541813-37542073 | Common:2; Rare:47 | ||||
| chr22:37544302-37544373 | Rare:7 | ||||
| chr22:37625057-37625267 | Rare:48 | ||||
| chr22:37769048-37769291 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:37805945-37806149 | Rare:67 | ||||
| chr22:37806296-37806478 | Common:3; Rare:32 | ||||
| chr22:37807230-37807270 | Rare:3 | ||||
| chr22:37807354-37807399 | Rare:10 |