| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136662686-136662978 | Common:1; Rare:71 | ||||
| chr9:136745890-136746216 | Common:1; Rare:85 | ||||
| chr9:137086823-137087131 | Common:1; Rare:130; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:137188547-137188723 | Common:2; Rare:90 | ||||
| chr9:137205480-137205758 | Common:1; Rare:100 | ||||
| chr9:137550355-137550477 | Rare:19 | ||||
| chr9:137618846-137619047 | Common:1; Rare:81 | ||||
| chrM:3167-3890 | |||||
| chrM:3902-4103 | |||||
| chrM:4312-5035 | |||||
| chrM:5195-5772 | |||||
| chrM:7566-7616 | |||||
| chrM:7624-8172 | |||||
| chrM:8207-8782 | |||||
| chrM:8836-9175 |