| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136724781-136724810 | Rare:9 | ||||
| chr9:136724855-136725177 | Common:4; Rare:65 | ||||
| chr9:136725746-136726039 | Common:5; Rare:68 | ||||
| chr9:136726303-136726374 | Rare:17 | ||||
| chr9:136727022-136727316 | Common:3; Rare:47 | ||||
| chr9:136840078-136840210 | Common:1; Rare:51 | ||||
| chr9:136847879-136848034 | Rare:46 | ||||
| chr9:136862903-136863448 | Common:2; Rare:157 | ||||
| chr9:136938427-136938650 | Common:2; Rare:50 | ||||
| chr9:137042925-137043248 | Common:1; Rare:116 | ||||
| chr9:137108227-137108453 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:137129664-137129890 | Common:3; Rare:76 | ||||
| chr9:137217363-137217500 | Rare:46 | ||||
| chr9:137270304-137270608 | Common:1; Rare:65 | ||||
| chr9:137607192-137607266 | Rare:14 |