| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34637720-34637924 | Rare:61 | ||||
| chr9:34665380-34665652 | Rare:88 | ||||
| chr9:35079753-35079839 | Rare:15 | ||||
| chr9:35103080-35103289 | Common:1; Rare:69 | ||||
| chr9:35489922-35490133 | Common:2; Rare:60 | ||||
| chr9:35657850-35658342 | Common:8; Rare:421; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35732082-35732683 | Common:5; Rare:168 | ||||
| chr9:35748859-35749378 | Common:3; Rare:171 | ||||
| chr9:35814983-35815293 | Rare:79 | ||||
| chr9:36190681-36191008 | Common:2; Rare:109 | ||||
| chr9:36258409-36258601 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37785015-37785115 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800707-37800794 | Rare:25 | ||||
| chr9:37904079-37904237 | Common:2; Rare:49 | ||||
| chr9:69759936-69760099 | Common:2; Rare:81 |