| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124815746-124815812 | Common:1; Rare:23 | ||||
| chr8:124848618-124848649 | Rare:7 | ||||
| chr8:129148529-129148714 | Common:3; Rare:42 | ||||
| chr8:143281614-143281803 | Common:3; Rare:49 | ||||
| chr8:143935980-143936090 | Rare:37; Clinvar (benign):1 | ||||
| chr8:144313784-144314454 | Common:3; Rare:327 | ||||
| chr8:144508226-144508267 | Rare:10 | ||||
| chr8:144700255-144700416 | Rare:28 | ||||
| chr8:144700482-144700697 | Common:3; Rare:47 | ||||
| chr8:145002821-145003038 | Common:2; Rare:80 | ||||
| chr9:72583-72677 | Rare:10 | ||||
| chr9:73851-74123 | Common:4; Rare:121 | ||||
| chr9:503947-504060 | Common:3; Rare:35 | ||||
| chr9:569244-569471 | Common:1; Rare:51 | ||||
| chr9:580397-580570 | Rare:57 |