| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130479284-130479904 | Common:2; Rare:187; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr9:130579428-130579689 | Common:7; Rare:106 | ||||
| chr9:130664147-130664269 | Rare:21 | ||||
| chr9:130693602-130693850 | Common:1; Rare:96 | ||||
| chr9:130835165-130835373 | Common:8; Rare:64 | ||||
| chr9:131125413-131125651 | Common:2; Rare:113 | ||||
| chr9:131531182-131531396 | Common:10; Rare:96 | ||||
| chr9:132354952-132355295 | Common:5; Rare:110 | ||||
| chr9:132669939-132670078 | Common:1; Rare:63 | ||||
| chr9:132670344-132670489 | Rare:49 | ||||
| chr9:132878282-132878385 | Common:1; Rare:36 | ||||
| chr9:133336125-133336319 | Common:1; Rare:83 | ||||
| chr9:133347980-133348276 | Common:3; Rare:110 | ||||
| chr9:133356431-133356619 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375999-133376340 | Common:1; Rare:125 |