| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127122606-127122961 | Common:3; Rare:92 | ||||
| chr9:127224379-127224652 | Rare:74 | ||||
| chr9:127424255-127424440 | Common:1; Rare:60 | ||||
| chr9:127451282-127451565 | Common:3; Rare:118; Clinvar (benign):1 | ||||
| chr9:127762292-127762557 | Common:2; Rare:60 | ||||
| chr9:128160046-128160420 | Common:2; Rare:91 | ||||
| chr9:128275897-128276302 | Common:5; Rare:176 | ||||
| chr9:128322410-128322628 | Common:1; Rare:61 | ||||
| chr9:128322751-128322880 | Common:2; Rare:62; Clinvar (benign):5 | ||||
| chr9:128371203-128371382 | Rare:60 | ||||
| chr9:128504601-128504791 | Rare:89; Clinvar:5 | ||||
| chr9:128552408-128552607 | Rare:75; Clinvar:1 | ||||
| chr9:128656650-128656816 | Common:2; Rare:74; Clinvar (pathogenic):1 | ||||
| chr9:128724095-128724464 | Common:2; Rare:121 | ||||
| chr9:128771854-128772005 | Rare:42 |