| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136944611-136944873 | Common:2; Rare:99 | ||||
| chr9:137028168-137028427 | Common:1; Rare:81 | ||||
| chr9:137046126-137046233 | Common:1; Rare:32 | ||||
| chr9:137046669-137046765 | Rare:26 | ||||
| chr9:137086826-137087146 | Common:1; Rare:136; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137188532-137188737 | Common:2; Rare:101 | ||||
| chr9:137205473-137205773 | Common:2; Rare:112 | ||||
| chr9:137423262-137423581 | Common:5; Rare:91 | ||||
| chr9:137551653-137551959 | Common:27; Rare:131 | ||||
| chr9:137578826-137578945 | Common:2; Rare:43 | ||||
| chr9:137618535-137619047 | Common:2; Rare:181 | ||||
| chr9:137666986-137667043 | Rare:13 | ||||
| chrM:3169-3531 | |||||
| chrM:3532-3550 | |||||
| chrM:3560-3670 |