| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34380831-34380956 | Common:1; Rare:58 | ||||
| chr9:34993921-34994223 | Rare:52 | ||||
| chr9:35341685-35341879 | Common:1; Rare:32 | ||||
| chr9:35519182-35519342 | Rare:15 | ||||
| chr9:35604021-35604365 | Common:3; Rare:95 | ||||
| chr9:35657724-35657764 | Common:1; Rare:26; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35907865-35907949 | Common:1; Rare:20 | ||||
| chr9:35909324-35909527 | Common:4; Rare:51 | ||||
| chr9:35909882-35910203 | Common:1; Rare:73 | ||||
| chr9:35929356-35929454 | Rare:15 | ||||
| chr9:36352980-36353246 | Rare:70 | ||||
| chr9:38650062-38650307 | Common:2; Rare:46 | ||||
| chr9:39464449-39464653 | Common:1; Rare:49 | ||||
| chr9:39809213-39809534 | Common:4; Rare:21 | ||||
| chr9:39809672-39809775 | Common:2; Rare:9 |