| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33290347-33290581 | Common:2; Rare:87 | ||||
| chr9:33473838-33474168 | Common:4; Rare:100 | ||||
| chr9:34048833-34049318 | Common:3; Rare:161 | ||||
| chr9:34178821-34179232 | Common:1; Rare:104 | ||||
| chr9:34329195-34329596 | Rare:126 | ||||
| chr9:34612014-34612223 | Common:9; Rare:76 | ||||
| chr9:34637736-34638108 | Common:3; Rare:96 | ||||
| chr9:34654428-34654581 | Common:1; Rare:28 | ||||
| chr9:34665351-34665628 | Rare:86 | ||||
| chr9:35072536-35072949 | Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35101709-35102351 | Common:2; Rare:170 | ||||
| chr9:35102683-35103228 | Common:2; Rare:161 | ||||
| chr9:35161782-35162130 | Common:4; Rare:99 | ||||
| chr9:35162283-35162323 | Rare:10 | ||||
| chr9:35657924-35658365 | Common:6; Rare:353; Clinvar:26; Clinvar (benign):13; Clinvar (pathogenic):36 |