| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:123601586-123601901 | Rare:65 | ||||
| chr7:123655779-123656231 | Common:2; Rare:128 | ||||
| chr7:123748887-123749257 | Common:3; Rare:133 | ||||
| chr7:124929799-124929929 | Common:3; Rare:44 | ||||
| chr7:127585566-127585686 | Common:2; Rare:42 | ||||
| chr7:127588291-127588508 | Rare:93 | ||||
| chr7:127651830-127652260 | Common:3; Rare:128 | ||||
| chr7:128409924-128410044 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455758-128455885 | Common:2; Rare:74 | ||||
| chr7:128830140-128830548 | Common:4; Rare:105 | ||||
| chr7:128830550-128830989 | Common:1; Rare:144; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr7:128840592-128840969 | Common:6; Rare:107; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr7:128841167-128841567 | Common:2; Rare:127; Clinvar:13; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr7:129054817-129055234 | Common:2; Rare:85 | ||||
| chr7:129434248-129434470 | Common:1; Rare:81 |