| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131125407-131125651 | Common:2; Rare:115 | ||||
| chr9:132406815-132406885 | Rare:24 | ||||
| chr9:132669952-132670078 | Common:1; Rare:57 | ||||
| chr9:133348070-133348253 | Common:2; Rare:70 | ||||
| chr9:133356467-133356616 | Common:1; Rare:69; Clinvar (benign):2 | ||||
| chr9:133376031-133376321 | Common:1; Rare:104 | ||||
| chr9:137086658-137087002 | Common:1; Rare:132; Clinvar:1 | ||||
| chr9:137188547-137188713 | Common:2; Rare:80 | ||||
| chr9:137618783-137619024 | Common:1; Rare:110 | ||||
| chrM:7467-7616 | |||||
| chrM:7894-8096 | |||||
| chrM:9185-9400 | |||||
| chrM:10173-10508 | |||||
| chrM:11144-11273 | |||||
| chrM:12808-13107 |