| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34126615-34126841 | Common:1; Rare:68 | ||||
| chr9:34178939-34179081 | Common:1; Rare:39 | ||||
| chr9:34329187-34329598 | Rare:130 | ||||
| chr9:34458533-34458794 | Common:1; Rare:66 | ||||
| chr9:34637526-34637924 | Common:1; Rare:119; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:34652007-34652217 | Rare:62 | ||||
| chr9:34665381-34665663 | Rare:91 | ||||
| chr9:34666021-34666136 | Common:1; Rare:22 | ||||
| chr9:35102172-35102472 | Rare:60 | ||||
| chr9:35102799-35103214 | Common:1; Rare:127 | ||||
| chr9:35162286-35162357 | Rare:25 | ||||
| chr9:35657846-35658376 | Common:8; Rare:441; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35689912-35690185 | Common:4; Rare:72; Clinvar:2 | ||||
| chr9:35698886-35699128 | Common:1; Rare:71 | ||||
| chr9:35732073-35732334 | Common:2; Rare:70 |