| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112379869-112380143 | Common:1; Rare:120 | ||||
| chr9:113221294-113221594 | Rare:93 | ||||
| chr9:113275558-113275689 | Common:1; Rare:46; Clinvar (pathogenic):1 | ||||
| chr9:122264762-122264916 | Common:2; Rare:47 | ||||
| chr9:127451344-127451510 | Common:2; Rare:72 | ||||
| chr9:128275941-128276288 | Common:4; Rare:163 | ||||
| chr9:128371181-128371383 | Rare:69 | ||||
| chr9:128947573-128947722 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129835225-129835408 | Common:1; Rare:78 | ||||
| chr9:130053854-130053929 | Common:1; Rare:24 | ||||
| chr9:133348080-133348246 | Common:1; Rare:65 | ||||
| chr9:133356470-133356589 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr9:137618818-137619024 | Common:1; Rare:92 | ||||
| chrM:6398-7211 | |||||
| chrM:15024-15240 |