| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33290255-33290570 | Common:3; Rare:107 | ||||
| chr9:33473863-33474143 | Common:2; Rare:83 | ||||
| chr9:34178928-34179090 | Common:1; Rare:44 | ||||
| chr9:34329186-34329598 | Rare:131 | ||||
| chr9:34458539-34458875 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:34612084-34612219 | Common:8; Rare:45 | ||||
| chr9:34652032-34652207 | Rare:50 | ||||
| chr9:34665381-34665665 | Rare:91 | ||||
| chr9:34665977-34666177 | Common:2; Rare:54 | ||||
| chr9:35079935-35080157 | Common:4; Rare:58; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35103073-35103297 | Common:1; Rare:83 | ||||
| chr9:35161819-35162065 | Common:4; Rare:72 | ||||
| chr9:35489881-35490139 | Common:2; Rare:76 | ||||
| chr9:35657801-35657818 | Rare:15; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr9:35657850-35658342 | Common:8; Rare:421; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 |