| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128684938-128685069 | Rare:22 | ||||
| chr9:128689516-128689638 | Rare:49 | ||||
| chr9:128724081-128724472 | Common:3; Rare:128 | ||||
| chr9:128787155-128787341 | Common:3; Rare:64 | ||||
| chr9:128881907-128882202 | Common:2; Rare:98 | ||||
| chr9:128921983-128922324 | Common:1; Rare:78 | ||||
| chr9:128947573-128947722 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129028096-129028174 | Rare:18 | ||||
| chr9:129080746-129081140 | Common:2; Rare:103 | ||||
| chr9:129098250-129098576 | Rare:90 | ||||
| chr9:129110614-129111029 | Common:5; Rare:126 | ||||
| chr9:129111267-129111468 | Common:2; Rare:72 | ||||
| chr9:129753018-129753185 | Rare:44 | ||||
| chr9:129803062-129803336 | Common:2; Rare:100 | ||||
| chr9:129835138-129835498 | Common:4; Rare:141 |