| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127803144-127803334 | Common:1; Rare:44 | ||||
| chr9:127877662-127877771 | Rare:21 | ||||
| chr9:127899562-127899743 | Rare:68 | ||||
| chr9:127930774-127930903 | Common:1; Rare:35 | ||||
| chr9:127937811-127937916 | Common:1; Rare:30; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128159996-128160413 | Common:3; Rare:101 | ||||
| chr9:128190434-128190721 | Rare:74 | ||||
| chr9:128191768-128191857 | Common:1; Rare:21 | ||||
| chr9:128275919-128276338 | Common:5; Rare:193 | ||||
| chr9:128322403-128322621 | Common:1; Rare:65 | ||||
| chr9:128322729-128322887 | Common:2; Rare:72; Clinvar (benign):5 | ||||
| chr9:128340407-128340728 | Common:2; Rare:104 | ||||
| chr9:128371235-128371432 | Rare:76 | ||||
| chr9:128504611-128504806 | Rare:90; Clinvar:5 | ||||
| chr9:128552413-128552602 | Rare:73; Clinvar:1 |