| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:23821812-23821950 | Rare:74 | ||||
| chr9:23826189-23826605 | Common:1; Rare:161 | ||||
| chr9:26892323-26892447 | Rare:56 | ||||
| chr9:26892734-26892927 | Common:1; Rare:91 | ||||
| chr9:26947105-26947348 | Common:1; Rare:83 | ||||
| chr9:26947409-26947602 | Common:1; Rare:58 | ||||
| chr9:26956225-26956470 | Common:2; Rare:90 | ||||
| chr9:26956663-26956771 | Common:4; Rare:26 | ||||
| chr9:26976210-26976720 | Common:1; Rare:100 | ||||
| chr9:27528928-27529630 | Common:12; Rare:169 | ||||
| chr9:27573399-27573572 | Common:6; Rare:97 | ||||
| chr9:27573789-27574051 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:32384393-32384670 | Common:1; Rare:86 | ||||
| chr9:32526178-32526374 | Common:3; Rare:58 | ||||
| chr9:32552253-32552380 | Rare:56 |