| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133348658-133349042 | Common:3; Rare:161 | ||||
| chr9:133356304-133356593 | Common:5; Rare:129; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:133376015-133376366 | Common:1; Rare:126 | ||||
| chr9:134641551-134641821 | Common:2; Rare:83; Clinvar (benign):1 | ||||
| chr9:136410372-136410664 | Common:6; Rare:123 | ||||
| chr9:136849596-136849760 | Common:1; Rare:65 | ||||
| chr9:136979960-136980272 | Rare:125 | ||||
| chr9:137086874-137087136 | Common:1; Rare:125; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137188547-137188672 | Common:2; Rare:56 | ||||
| chr9:137205480-137205697 | Common:1; Rare:63 | ||||
| chr9:137618796-137619031 | Common:1; Rare:106 | ||||
| chrM:3168-3817 | |||||
| chrM:4320-4332 | |||||
| chrM:5367-6280 | |||||
| chrM:9190-9708 |