| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136944604-136944864 | Common:1; Rare:101 | ||||
| chr9:137070555-137070725 | Common:2; Rare:32 | ||||
| chr9:137086692-137087108 | Common:1; Rare:167; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137188538-137188736 | Common:2; Rare:97 | ||||
| chr9:137200734-137201021 | Common:3; Rare:82 | ||||
| chr9:137204466-137204554 | Rare:17 | ||||
| chr9:137204660-137204810 | Common:1; Rare:28 | ||||
| chr9:137205633-137205735 | Rare:40 | ||||
| chr9:137277635-137277826 | Common:1; Rare:46 | ||||
| chr9:137423134-137423237 | Rare:36 | ||||
| chr9:137423247-137423265 | Rare:5 | ||||
| chr9:137578864-137579069 | Common:2; Rare:67 | ||||
| chr9:137590498-137590669 | Common:1; Rare:69 | ||||
| chr9:137618797-137619029 | Common:1; Rare:105 | ||||
| chrM:2792-2889 |