| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95086117-95086347 | Common:1; Rare:58 | ||||
| chr9:95098264-95098536 | Common:2; Rare:66 | ||||
| chr9:95109242-95109417 | Rare:34 | ||||
| chr9:95111486-95111778 | Common:2; Rare:82; Clinvar:14; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr9:95426753-95426913 | Common:3; Rare:64 | ||||
| chr9:95481963-95482165 | Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:96116386-96116422 | Rare:14 | ||||
| chr9:97238254-97238527 | Common:5; Rare:78 | ||||
| chr9:97645527-97645633 | Rare:14 | ||||
| chr9:97662679-97663046 | Rare:75 | ||||
| chr9:97664205-97664451 | Common:1; Rare:60 | ||||
| chr9:97669332-97669684 | Common:3; Rare:72 | ||||
| chr9:97687094-97687432 | Common:1; Rare:79; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr9:97693647-97693872 | Common:1; Rare:54; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr9:98944276-98944455 | Rare:36 |