| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34612090-34612182 | Common:1; Rare:28 | ||||
| chr9:34646296-34646786 | Common:2; Rare:120; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34665373-34665665 | Rare:94 | ||||
| chr9:35072367-35072675 | Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35103100-35103266 | Common:1; Rare:51 | ||||
| chr9:35161782-35162038 | Common:4; Rare:71 | ||||
| chr9:35657841-35658342 | Common:9; Rare:425; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35732083-35732671 | Common:4; Rare:164 | ||||
| chr9:35748941-35749354 | Common:2; Rare:148 | ||||
| chr9:36190725-36190985 | Common:1; Rare:85 | ||||
| chr9:36258430-36258622 | Common:2; Rare:45; Clinvar:1 | ||||
| chr9:37800707-37800829 | Rare:37 | ||||
| chr9:37904067-37904217 | Rare:52 | ||||
| chr9:37904346-37904414 | Rare:22 | ||||
| chr9:68779966-68780082 | Common:1; Rare:35 |