| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:23850341-23850618 | Rare:50 | ||||
| chr9:29212176-29212486 | Common:2; Rare:85 | ||||
| chr9:29212965-29213052 | Rare:24 | ||||
| chr9:29213951-29214336 | Common:3; Rare:106 | ||||
| chr9:32550821-32551150 | Common:1; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33818730-33818780 | Common:1; Rare:9 | ||||
| chr9:34380828-34380948 | Common:1; Rare:54 | ||||
| chr9:35341751-35341919 | Common:1; Rare:27 | ||||
| chr9:35604021-35604431 | Common:3; Rare:109 | ||||
| chr9:35686383-35686505 | Common:2; Rare:18 | ||||
| chr9:35749949-35749993 | Rare:3 | ||||
| chr9:36352578-36352778 | Common:1; Rare:49 | ||||
| chr9:37079590-37080021 | Common:5; Rare:105 | ||||
| chr9:38414287-38414460 | Common:1; Rare:36 | ||||
| chr9:38622542-38622579 | Rare:8 |