| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128947608-128947717 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129835241-129835472 | Common:2; Rare:87 | ||||
| chr9:130053847-130053929 | Common:1; Rare:26 | ||||
| chr9:132669992-132670036 | Common:1; Rare:22 | ||||
| chr9:133030885-133031004 | Rare:40 | ||||
| chr9:133348087-133348260 | Common:1; Rare:74 | ||||
| chr9:133356470-133356607 | Common:1; Rare:61; Clinvar (benign):2 | ||||
| chr9:133376015-133376346 | Common:1; Rare:120 | ||||
| chr9:136410346-136410664 | Common:6; Rare:132 | ||||
| chr9:137188552-137188723 | Common:2; Rare:88 | ||||
| chr9:137618824-137619024 | Common:1; Rare:88 | ||||
| chrM:3204-3404 | |||||
| chrM:7348-7597 | |||||
| chrM:7824-8148 | |||||
| chrM:9090-9298 |