| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33025061-33025312 | Common:6; Rare:105 | ||||
| chr9:33166881-33166919 | Rare:17 | ||||
| chr9:33167184-33167502 | Common:1; Rare:107; Clinvar:5 | ||||
| chr9:33264718-33265072 | Rare:91 | ||||
| chr9:33290333-33290565 | Common:2; Rare:84 | ||||
| chr9:33402426-33402664 | Rare:45 | ||||
| chr9:33795421-33795625 | Common:15; Rare:35 | ||||
| chr9:33796023-33796202 | Common:1; Rare:26 | ||||
| chr9:33798328-33798539 | Common:1; Rare:62 | ||||
| chr9:34178935-34179061 | Common:1; Rare:34 | ||||
| chr9:34329250-34329593 | Rare:102 | ||||
| chr9:34458540-34458833 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:34665363-34665654 | Rare:94 | ||||
| chr9:35072468-35072868 | Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35103073-35103288 | Common:1; Rare:76 |