| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127802714-127803047 | Common:3; Rare:90 | ||||
| chr9:127824889-127825142 | Rare:59; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:127854642-127854877 | Rare:50; Clinvar:5 | ||||
| chr9:127897321-127897536 | Common:1; Rare:47 | ||||
| chr9:127899518-127899743 | Rare:82 | ||||
| chr9:127937828-127937923 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128098289-128098582 | Common:1; Rare:67 | ||||
| chr9:128098812-128099059 | Common:1; Rare:53 | ||||
| chr9:128160008-128160363 | Common:2; Rare:81 | ||||
| chr9:128191515-128191642 | Rare:34 | ||||
| chr9:128275910-128276307 | Common:5; Rare:173 | ||||
| chr9:128322410-128322512 | Common:1; Rare:34 | ||||
| chr9:128322713-128322912 | Common:2; Rare:93; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:128371225-128371401 | Rare:66 | ||||
| chr9:128455963-128456203 | Common:1; Rare:80 |