| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:27573426-27573530 | Common:5; Rare:55 | ||||
| chr9:27573709-27573972 | Common:2; Rare:85; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32552557-32552628 | Common:1; Rare:14; Clinvar:2 | ||||
| chr9:32572981-32573245 | Common:3; Rare:91 | ||||
| chr9:33001560-33001751 | Common:3; Rare:93; Clinvar (benign):3 | ||||
| chr9:33025029-33025457 | Common:8; Rare:164 | ||||
| chr9:33025660-33025920 | Common:3; Rare:99 | ||||
| chr9:33076592-33076861 | Common:2; Rare:85 | ||||
| chr9:33264256-33264305 | Rare:18 | ||||
| chr9:33264932-33265129 | Rare:61 | ||||
| chr9:33290350-33290571 | Common:2; Rare:83 | ||||
| chr9:33473843-33474126 | Common:4; Rare:89 | ||||
| chr9:33750613-33750690 | Rare:27 | ||||
| chr9:34048853-34048992 | Common:2; Rare:58 | ||||
| chr9:34049181-34049308 | Common:1; Rare:31 |