| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94374286-94374601 | Common:4; Rare:213 | ||||
| chr9:94726518-94726739 | Common:1; Rare:115 | ||||
| chr9:95004601-95005053 | Rare:316 | ||||
| chr9:95316840-95317090 | Common:2; Rare:112 | ||||
| chr9:95317100-95317480 | Common:11; Rare:230 | ||||
| chr9:95317653-95317876 | Common:2; Rare:122; Clinvar:4 | ||||
| chr9:95505857-95506315 | Common:4; Rare:290 | ||||
| chr9:95507220-95507740 | Rare:245 | ||||
| chr9:95875434-95875741 | Common:2; Rare:211 | ||||
| chr9:95875840-95876100 | Common:11; Rare:145; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:96383526-96383878 | Common:6; Rare:185 | ||||
| chr9:96418314-96418597 | Common:4; Rare:117 | ||||
| chr9:96418600-96419080 | Common:5; Rare:244 | ||||
| chr9:96449951-96450268 | Common:3; Rare:112 | ||||
| chr9:96566691-96566815 | Common:1; Rare:48 |