| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31713330-31713613 | Rare:51 | ||||
| chr20:31895121-31895382 | Common:2; Rare:40 | ||||
| chr20:32036884-32037044 | Common:1; Rare:26 | ||||
| chr20:32091974-32092221 | Common:1; Rare:51 | ||||
| chr20:32190277-32190493 | Common:2; Rare:45 | ||||
| chr20:32205559-32205721 | Rare:26 | ||||
| chr20:32484624-32484787 | Rare:32 | ||||
| chr20:32484997-32485107 | Common:1; Rare:29 | ||||
| chr20:32574552-32574684 | Common:1; Rare:28 | ||||
| chr20:33443356-33443387 | Rare:10; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:33555007-33555233 | Rare:31 | ||||
| chr20:33667320-33667428 | Common:1; Rare:18 | ||||
| chr20:33667999-33668257 | Rare:133 | ||||
| chr20:33672867-33673137 | Rare:59 | ||||
| chr20:33685426-33685541 | Rare:29 |