| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127517730-127517936 | Rare:57 | ||||
| chr9:127599457-127599578 | Common:2; Rare:15 | ||||
| chr9:127792266-127792345 | Rare:17 | ||||
| chr9:127795590-127795816 | Common:2; Rare:41 | ||||
| chr9:127795997-127796293 | Common:3; Rare:65 | ||||
| chr9:127819621-127820061 | Rare:113; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr9:127868054-127868387 | Common:5; Rare:86; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:128101447-128101731 | Common:1; Rare:52 | ||||
| chr9:128224094-128224256 | Rare:42; Clinvar (benign):4 | ||||
| chr9:128268286-128268453 | Common:1; Rare:49 | ||||
| chr9:128268460-128268788 | Common:2; Rare:67 | ||||
| chr9:128617377-128617664 | Common:3; Rare:61; Clinvar (benign):4 | ||||
| chr9:128630280-128630376 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:128684413-128684537 | Rare:25 | ||||
| chr9:128693783-128693977 | Rare:65; Clinvar:1 |