| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130712960-130713086 | Common:1; Rare:41 | ||||
| chr9:130780971-130781023 | Rare:6 | ||||
| chr9:131373417-131373671 | Common:1; Rare:57 | ||||
| chr9:131627955-131628276 | Common:2; Rare:72 | ||||
| chr9:131676826-131676982 | Common:2; Rare:41 | ||||
| chr9:132902681-132902903 | Rare:40; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:133273457-133273695 | Common:2; Rare:36 | ||||
| chr9:133273782-133273912 | Common:1; Rare:26 | ||||
| chr9:136670772-136670980 | Common:1; Rare:52 | ||||
| chr9:136673909-136673989 | Rare:24; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr9:136693701-136694024 | Common:1; Rare:56 | ||||
| chr9:136802559-136802690 | Common:1; Rare:43 | ||||
| chr9:136803088-136803097 | |||||
| chr9:136803223-136803509 | Common:8; Rare:78 | ||||
| chr9:136804315-136804546 | Common:5; Rare:55 |