| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127787951-127788223 | Common:2; Rare:87 | ||||
| chr9:127824889-127825121 | Rare:56; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:127899518-127899742 | Rare:81 | ||||
| chr9:127916994-127917261 | Rare:80 | ||||
| chr9:127937828-127937932 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128098272-128098539 | Common:1; Rare:53 | ||||
| chr9:128160024-128160383 | Common:2; Rare:86 | ||||
| chr9:128191515-128191651 | Rare:35 | ||||
| chr9:128191764-128191826 | Common:1; Rare:14 | ||||
| chr9:128275909-128276307 | Common:5; Rare:173 | ||||
| chr9:128322410-128322486 | Rare:31 | ||||
| chr9:128322751-128322880 | Common:2; Rare:62; Clinvar (benign):5 | ||||
| chr9:128371235-128371382 | Rare:47 | ||||
| chr9:128504627-128504764 | Rare:54; Clinvar:5 | ||||
| chr9:128552408-128552611 | Rare:79; Clinvar:1 |