| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127778664-127778873 | Common:1; Rare:36 | ||||
| chr9:127802714-127803047 | Common:3; Rare:90 | ||||
| chr9:127899562-127899727 | Rare:61 | ||||
| chr9:127916980-127917261 | Common:1; Rare:85 | ||||
| chr9:127937824-127937992 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:128160034-128160423 | Common:2; Rare:94 | ||||
| chr9:128275919-128276302 | Common:5; Rare:172 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322729-128322880 | Common:2; Rare:68; Clinvar (benign):5 | ||||
| chr9:128371193-128371422 | Rare:89 | ||||
| chr9:128455963-128456174 | Common:1; Rare:66 | ||||
| chr9:128504598-128504780 | Rare:84; Clinvar:5 | ||||
| chr9:128552394-128552611 | Rare:81; Clinvar:1 | ||||
| chr9:128656662-128656990 | Common:1; Rare:110; Clinvar (pathogenic):1 | ||||
| chr9:128683645-128683934 | Rare:80 |