| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:27003766-27003988 | Rare:42 | ||||
| chr9:32405293-32405553 | Common:1; Rare:46 | ||||
| chr9:32440392-32440486 | Common:1; Rare:25 | ||||
| chr9:33752285-33752580 | Common:1; Rare:54 | ||||
| chr9:33818627-33818944 | Common:1; Rare:59 | ||||
| chr9:33916878-33917054 | Rare:53 | ||||
| chr9:34380624-34380937 | Common:1; Rare:105 | ||||
| chr9:35604027-35604371 | Common:3; Rare:91 | ||||
| chr9:35724576-35724960 | Common:1; Rare:86 | ||||
| chr9:35739765-35740013 | Common:2; Rare:62; Clinvar (benign):2 | ||||
| chr9:36219994-36220147 | Common:1; Rare:29; Clinvar:4 | ||||
| chr9:37080125-37080372 | Common:1; Rare:81 | ||||
| chr9:37777452-37777544 | Rare:33 | ||||
| chr9:39809191-39809517 | Common:4; Rare:24 | ||||
| chr9:39809851-39809865 | Common:1 |