| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35385728-35385999 | Common:3; Rare:50 | ||||
| chr9:35592884-35592886 | |||||
| chr9:35684248-35684515 | Rare:60; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:35718381-35718658 | Rare:50 | ||||
| chr9:35720732-35720824 | Rare:27 | ||||
| chr9:35733216-35733480 | Rare:93 | ||||
| chr9:35742817-35743107 | Common:2; Rare:56 | ||||
| chr9:35751747-35752022 | Common:2; Rare:82 | ||||
| chr9:35769955-35769970 | Rare:4 | ||||
| chr9:35971123-35971419 | Common:2; Rare:49 | ||||
| chr9:36037968-36037996 | Rare:5 | ||||
| chr9:36472688-36472895 | Common:2; Rare:42 | ||||
| chr9:37079796-37080034 | Common:4; Rare:79 | ||||
| chr9:37086925-37087360 | Common:5; Rare:65 | ||||
| chr9:37087436-37087569 | Rare:27 |