| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37120415-37120636 | Common:1; Rare:82 | ||||
| chr9:37422557-37422753 | Common:2; Rare:98 | ||||
| chr9:37465259-37465585 | Common:3; Rare:106 | ||||
| chr9:37465790-37466009 | Common:3; Rare:56 | ||||
| chr9:37485706-37486045 | Common:4; Rare:117 | ||||
| chr9:37576211-37576539 | Common:1; Rare:88 | ||||
| chr9:37592530-37592755 | Common:2; Rare:68 | ||||
| chr9:37753540-37754100 | Common:10; Rare:235 | ||||
| chr9:37785004-37785159 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800639-37800841 | Common:2; Rare:71 | ||||
| chr9:37903490-37903940 | Common:1; Rare:138 | ||||
| chr9:37904334-37904489 | Rare:53 | ||||
| chr9:38069199-38069342 | Common:3; Rare:54 | ||||
| chr9:38069710-38070020 | Common:4; Rare:70 | ||||
| chr9:38392504-38392778 | Common:2; Rare:75 |