| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35829124-35829280 | Common:1; Rare:43 | ||||
| chr9:35905890-35906218 | Common:3; Rare:73 | ||||
| chr9:36190720-36191058 | Common:2; Rare:105 | ||||
| chr9:36258374-36258646 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400837-36400995 | Common:3; Rare:71 | ||||
| chr9:36401172-36401282 | Rare:34 | ||||
| chr9:36572770-36572902 | Rare:34 | ||||
| chr9:37422591-37422824 | Common:2; Rare:107; Clinvar:1 | ||||
| chr9:37464970-37465033 | Common:1; Rare:18 | ||||
| chr9:37576211-37576420 | Rare:53 | ||||
| chr9:37784988-37785149 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800690-37800842 | Common:1; Rare:48 | ||||
| chr9:37801380-37801758 | Common:3; Rare:89 | ||||
| chr9:37904067-37904241 | Common:2; Rare:56 | ||||
| chr9:37904346-37904463 | Rare:41 |