| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:29213582-29213630 | Rare:17 | ||||
| chr9:30575003-30575150 | Common:1; Rare:48 | ||||
| chr9:31724510-31724643 | Rare:26 | ||||
| chr9:31848600-31848680 | Common:2; Rare:28 | ||||
| chr9:32448744-32449043 | Common:6; Rare:103 | ||||
| chr9:32550824-32551198 | Common:1; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:32551660-32551742 | Common:1; Rare:11 | ||||
| chr9:32738831-32739009 | Common:1; Rare:34 | ||||
| chr9:32761190-32761273 | Rare:17 | ||||
| chr9:32906728-32906996 | Common:4; Rare:51 | ||||
| chr9:33267086-33267244 | Rare:23 | ||||
| chr9:33375330-33375663 | Common:1; Rare:65 | ||||
| chr9:33511078-33511188 | Common:1; Rare:42 | ||||
| chr9:33677144-33677256 | Common:4; Rare:34 | ||||
| chr9:33749399-33749713 | Common:3; Rare:79 |