| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:27573732-27573972 | Common:2; Rare:76; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384471-32384732 | Common:1; Rare:93 | ||||
| chr9:32526155-32526354 | Common:4; Rare:64 | ||||
| chr9:32552557-32552676 | Common:1; Rare:22; Clinvar:2 | ||||
| chr9:33025056-33025407 | Common:7; Rare:138 | ||||
| chr9:33166780-33166989 | Rare:74; Clinvar:2 | ||||
| chr9:33167296-33167579 | Rare:105; Clinvar:1 | ||||
| chr9:33264626-33264916 | Common:1; Rare:81 | ||||
| chr9:33290363-33290595 | Common:2; Rare:89 | ||||
| chr9:33473852-33474140 | Common:4; Rare:87 | ||||
| chr9:33817640-33817943 | Common:1; Rare:87 | ||||
| chr9:34048851-34048982 | Common:2; Rare:54 | ||||
| chr9:34049175-34049263 | Common:1; Rare:22 | ||||
| chr9:34126352-34126777 | Rare:151 | ||||
| chr9:34178933-34179090 | Common:1; Rare:43 |