| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137086731-137087146 | Common:2; Rare:166; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137188547-137188713 | Common:2; Rare:80 | ||||
| chr9:137188851-137189166 | Common:2; Rare:112 | ||||
| chr9:137205651-137205747 | Rare:42 | ||||
| chr9:137277568-137277731 | Rare:41 | ||||
| chr9:137550355-137550491 | Rare:20 | ||||
| chr9:137551647-137551952 | Common:28; Rare:131 | ||||
| chr9:137578828-137579016 | Common:2; Rare:63 | ||||
| chr9:137618831-137619047 | Common:1; Rare:92 | ||||
| chrM:4305-4394 | |||||
| chrM:4472-5362 | |||||
| chrM:5426-5772 | |||||
| chrM:7360-7542 | |||||
| chrM:7566-8295 | |||||
| chrM:9810-10414 |