| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35829197-35829290 | Rare:30 | ||||
| chr9:35906184-35906279 | Rare:24 | ||||
| chr9:36190715-36191272 | Common:3; Rare:173 | ||||
| chr9:36258367-36258607 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36276952-36277303 | Common:3; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:37120174-37120618 | Common:2; Rare:140 | ||||
| chr9:37422613-37422809 | Common:2; Rare:95; Clinvar:1 | ||||
| chr9:37464961-37465030 | Common:1; Rare:21 | ||||
| chr9:37485737-37486030 | Common:3; Rare:102 | ||||
| chr9:37576202-37576406 | Rare:51 | ||||
| chr9:37592492-37592648 | Common:2; Rare:62 | ||||
| chr9:37785004-37785126 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800696-37800837 | Rare:43 | ||||
| chr9:37801444-37801604 | Common:2; Rare:36 | ||||
| chr9:37904066-37904478 | Common:3; Rare:135 |