| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133336140-133336345 | Common:1; Rare:80 | ||||
| chr9:133348043-133348328 | Common:3; Rare:123 | ||||
| chr9:133356449-133356618 | Common:1; Rare:80; Clinvar (benign):2 | ||||
| chr9:133375959-133376366 | Common:3; Rare:146 | ||||
| chr9:136410410-136410671 | Common:6; Rare:113 | ||||
| chr9:136662650-136663087 | Common:2; Rare:103 | ||||
| chr9:137087034-137087168 | Common:1; Rare:61; Clinvar:3 | ||||
| chr9:137188547-137188713 | Common:2; Rare:80 | ||||
| chr9:137618824-137619044 | Common:1; Rare:97 | ||||
| chrM:3168-3219 | |||||
| chrM:5577-5590 | |||||
| chrM:5881-5926 | |||||
| chrM:6393-7304 | |||||
| chrM:7400-7586 | |||||
| chrM:7913-8152 |