| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130053877-130053939 | Common:1; Rare:22 | ||||
| chr9:130579456-130579686 | Common:6; Rare:98 | ||||
| chr9:131125435-131125651 | Common:1; Rare:104 | ||||
| chr9:131531188-131531342 | Common:9; Rare:69 | ||||
| chr9:133348037-133348258 | Common:3; Rare:86 | ||||
| chr9:133356452-133356593 | Common:1; Rare:64; Clinvar (benign):2 | ||||
| chr9:133375985-133376340 | Common:3; Rare:130 | ||||
| chr9:134641551-134641812 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr9:136800134-136800349 | Common:4; Rare:65 | ||||
| chr9:136944608-136944934 | Common:2; Rare:119 | ||||
| chr9:137618833-137619029 | Common:1; Rare:83 | ||||
| chrM:3168-3460 | |||||
| chrM:5577-5590 | |||||
| chrM:5896-6347 | |||||
| chrM:6352-7296 |