| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37800685-37800924 | Common:2; Rare:84 | ||||
| chr9:37801380-37801543 | Common:2; Rare:48 | ||||
| chr9:37904024-37904200 | Rare:55 | ||||
| chr9:37904338-37904414 | Rare:26 | ||||
| chr9:68779818-68780114 | Common:4; Rare:102 | ||||
| chr9:69672316-69672604 | Common:1; Rare:91 | ||||
| chr9:69759907-69760140 | Common:3; Rare:101 | ||||
| chr9:70258814-70259077 | Common:4; Rare:124 | ||||
| chr9:71911126-71911533 | Common:3; Rare:125 | ||||
| chr9:72364505-72364805 | Common:4; Rare:100 | ||||
| chr9:72365195-72365423 | Common:2; Rare:79 | ||||
| chr9:74497123-74497346 | Common:3; Rare:50 | ||||
| chr9:75088057-75088715 | Common:4; Rare:215 | ||||
| chr9:76394317-76394566 | Common:6; Rare:86 | ||||
| chr9:77177438-77177699 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):2 |