| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36258388-36258607 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37422576-37422735 | Common:2; Rare:83 | ||||
| chr9:37465267-37465602 | Common:3; Rare:105 | ||||
| chr9:37800696-37800837 | Rare:43 | ||||
| chr9:37801398-37801446 | Rare:16 | ||||
| chr9:37904045-37904247 | Common:2; Rare:62 | ||||
| chr9:37904316-37904463 | Rare:57 | ||||
| chr9:38392505-38392806 | Common:2; Rare:81 | ||||
| chr9:66900522-66900804 | Common:3; Rare:87 | ||||
| chr9:68356354-68356659 | Common:7; Rare:57 | ||||
| chr9:68356664-68356822 | Common:1; Rare:42 | ||||
| chr9:68356922-68357386 | Common:5; Rare:151 | ||||
| chr9:69759896-69760124 | Common:2; Rare:98 | ||||
| chr9:70044030-70044231 | Rare:42 | ||||
| chr9:70168414-70168795 | Common:2; Rare:74 |