| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133417981-133418309 | Common:4; Rare:75 | ||||
| chr9:134641551-134641809 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr9:136410393-136410680 | Common:6; Rare:124 | ||||
| chr9:136665568-136665817 | Common:2; Rare:66 | ||||
| chr9:136849587-136849770 | Common:1; Rare:69 | ||||
| chr9:136886249-136886533 | Common:2; Rare:83 | ||||
| chr9:137040538-137040688 | Rare:69 | ||||
| chr9:137188541-137188717 | Common:2; Rare:88 | ||||
| chr9:137205422-137205758 | Common:1; Rare:125 | ||||
| chr9:137551634-137551972 | Common:29; Rare:144 | ||||
| chr9:137578864-137579009 | Common:2; Rare:48 | ||||
| chr9:137618797-137619044 | Common:1; Rare:112 | ||||
| chrM:3150-3940 | |||||
| chrM:5577-5772 | |||||
| chrM:7398-7775 |