| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:16871937-16872147 | Rare:66 | ||||
| chr9:19126396-19126734 | Common:2; Rare:88 | ||||
| chr9:19128625-19128918 | Common:4; Rare:66 | ||||
| chr9:19378366-19378922 | Common:1; Rare:163 | ||||
| chr9:25677448-25677715 | Common:4; Rare:123 | ||||
| chr9:27460680-27460978 | Common:3; Rare:63 | ||||
| chr9:32418085-32418399 | Common:2; Rare:82 | ||||
| chr9:32418759-32419052 | Rare:59 | ||||
| chr9:32424408-32424638 | Rare:50 | ||||
| chr9:32436114-32436352 | Common:1; Rare:75 | ||||
| chr9:32550838-32551144 | Common:1; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33036753-33037112 | Common:2; Rare:84 | ||||
| chr9:33165801-33166013 | Common:1; Rare:39 | ||||
| chr9:33911777-33912088 | Common:1; Rare:62 | ||||
| chr9:34380816-34380930 | Common:1; Rare:43 |