| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:32552542-32552653 | Common:1; Rare:21; Clinvar:2 | ||||
| chr9:32573064-32573311 | Common:4; Rare:89 | ||||
| chr9:33001522-33001793 | Common:3; Rare:132; Clinvar (benign):4 | ||||
| chr9:33025006-33025333 | Common:7; Rare:133 | ||||
| chr9:33076596-33076860 | Common:2; Rare:84 | ||||
| chr9:33167314-33167542 | Rare:82 | ||||
| chr9:33264672-33265076 | Common:1; Rare:109 | ||||
| chr9:33290347-33290568 | Common:2; Rare:83 | ||||
| chr9:33447500-33447820 | Common:3; Rare:89 | ||||
| chr9:33473857-33474188 | Common:3; Rare:98 | ||||
| chr9:33524159-33524289 | Rare:34 | ||||
| chr9:33524310-33525012 | Common:11; Rare:239 | ||||
| chr9:33816863-33817337 | Common:2; Rare:139 | ||||
| chr9:33817462-33817900 | Common:2; Rare:149 | ||||
| chr9:33817973-33818209 | Rare:64 |