| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133417917-133418312 | Common:4; Rare:100 | ||||
| chr9:133479092-133479386 | Common:1; Rare:78 | ||||
| chr9:133738326-133738455 | Common:1; Rare:38 | ||||
| chr9:134135250-134135382 | Common:1; Rare:28 | ||||
| chr9:136373590-136373769 | Rare:35; Clinvar:4 | ||||
| chr9:136410390-136410721 | Common:7; Rare:147 | ||||
| chr9:137086674-137087010 | Common:1; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:137188538-137188713 | Common:2; Rare:83 | ||||
| chr9:137205376-137205747 | Common:1; Rare:133 | ||||
| chr9:137225106-137225188 | Common:2; Rare:37 | ||||
| chr9:137618764-137619038 | Common:1; Rare:125 | ||||
| chrM:3168-3437 | |||||
| chrM:5576-5600 | |||||
| chrM:5891-6280 | |||||
| chrM:6308-7277 |