| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:135961172-135961538 | Common:6; Rare:133 | ||||
| chr9:136410383-136410678 | Common:6; Rare:126 | ||||
| chr9:136886249-136886540 | Common:2; Rare:85 | ||||
| chr9:136944608-136944886 | Common:2; Rare:105 | ||||
| chr9:137086797-137087119 | Common:1; Rare:131; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137188537-137188723 | Common:2; Rare:94 | ||||
| chr9:137205473-137205757 | Common:1; Rare:100 | ||||
| chr9:137551647-137551948 | Common:28; Rare:129 | ||||
| chr9:137618774-137619041 | Common:1; Rare:120 | ||||
| chr9:137667146-137667328 | Common:1; Rare:40 | ||||
| chrM:3167-3376 | |||||
| chrM:3560-3792 | |||||
| chrM:4320-4332 | |||||
| chrM:4862-5140 | |||||
| chrM:5576-6170 |