| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128692709-128692979 | Rare:53 | ||||
| chr9:128724102-128724464 | Common:2; Rare:116 | ||||
| chr9:128881902-128882192 | Common:1; Rare:94 | ||||
| chr9:128947531-128947745 | Common:2; Rare:100; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:129110661-129110977 | Common:4; Rare:77 | ||||
| chr9:129802887-129803221 | Common:2; Rare:99 | ||||
| chr9:129835134-129835487 | Common:3; Rare:140 | ||||
| chr9:130042985-130043304 | Common:2; Rare:95 | ||||
| chr9:130053846-130053972 | Common:1; Rare:52 | ||||
| chr9:130579446-130579724 | Common:6; Rare:108 | ||||
| chr9:130693502-130693789 | Rare:80 | ||||
| chr9:130835136-130835309 | Rare:51 | ||||
| chr9:131125422-131125655 | Common:2; Rare:110 | ||||
| chr9:131502870-131503052 | Rare:64; Clinvar:3 | ||||
| chr9:132354939-132355240 | Common:4; Rare:98 |