| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130053854-130053933 | Common:1; Rare:24 | ||||
| chr9:130579446-130579673 | Common:5; Rare:91 | ||||
| chr9:131096221-131096585 | Common:4; Rare:97 | ||||
| chr9:132354955-132355186 | Common:3; Rare:75 | ||||
| chr9:133348034-133348246 | Common:3; Rare:78 | ||||
| chr9:133356470-133356589 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr9:133376007-133376340 | Common:1; Rare:123 | ||||
| chr9:133524925-133525104 | Common:1; Rare:25 | ||||
| chr9:136410326-136410667 | Common:6; Rare:143 | ||||
| chr9:137188547-137188737 | Common:2; Rare:94 | ||||
| chr9:137205468-137205726 | Common:1; Rare:81 | ||||
| chr9:137618797-137619031 | Common:1; Rare:105 | ||||
| chrM:3566-3915 | |||||
| chrM:5450-5639 | |||||
| chrM:7467-7626 |