Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:133336146-133336351 | Common:1; Rare:80 | ||||
chr9:133348039-133348258 | Common:2; Rare:86 | ||||
chr9:133356443-133356618 | Common:1; Rare:82; Clinvar (benign):2 | ||||
chr9:133375959-133376377 | Common:4; Rare:150 | ||||
chr9:136410417-136410666 | Common:6; Rare:108 | ||||
chr9:137188547-137188713 | Common:2; Rare:80 | ||||
chr9:137618813-137619029 | Common:1; Rare:97 | ||||
chrM:3119-3219 | |||||
chrM:4327-4601 | |||||
chrM:5560-5753 | |||||
chrM:5892-5934 | |||||
chrM:6294-6363 | |||||
chrM:6372-7314 | |||||
chrM:7396-7586 | |||||
chrM:8735-9013 |