| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127905298-127905421 | Common:1; Rare:21 | ||||
| chr9:127916981-127917246 | Common:1; Rare:77 | ||||
| chr9:128160107-128160410 | Common:2; Rare:79 | ||||
| chr9:128191453-128191668 | Rare:64 | ||||
| chr9:128275909-128276302 | Common:5; Rare:172 | ||||
| chr9:128340442-128340579 | Common:1; Rare:48 | ||||
| chr9:128371178-128371404 | Rare:87 | ||||
| chr9:128552040-128552158 | Common:1; Rare:34 | ||||
| chr9:128552284-128552667 | Common:1; Rare:140; Clinvar:5; Clinvar (benign):2 | ||||
| chr9:128656624-128657067 | Common:2; Rare:142; Clinvar (pathogenic):1 | ||||
| chr9:128683635-128683930 | Rare:80 | ||||
| chr9:128688918-128689242 | Rare:127 | ||||
| chr9:128692709-128692979 | Rare:53 | ||||
| chr9:128724097-128724464 | Common:2; Rare:120 | ||||
| chr9:128771839-128771980 | Rare:40 |