| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:6645692-6645912 | Common:1; Rare:71 | ||||
| chr9:6757552-6757672 | Common:1; Rare:47 | ||||
| chr9:13279584-13279811 | Common:2; Rare:72 | ||||
| chr9:15307204-15307444 | Common:2; Rare:118 | ||||
| chr9:15422556-15422898 | Common:1; Rare:152 | ||||
| chr9:15510956-15511097 | Rare:53 | ||||
| chr9:15552864-15552944 | Common:1; Rare:32 | ||||
| chr9:16870653-16870853 | Rare:98 | ||||
| chr9:19102786-19103070 | Common:3; Rare:114 | ||||
| chr9:19127467-19127581 | Common:1; Rare:36 | ||||
| chr9:19380190-19380370 | Common:4; Rare:86 | ||||
| chr9:19408744-19408936 | Common:5; Rare:74 | ||||
| chr9:20658195-20658359 | Common:4; Rare:60 | ||||
| chr9:20684047-20684284 | Common:4; Rare:91 | ||||
| chr9:21802515-21802696 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 |