| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:122144207-122144437 | Common:1; Rare:48 | ||||
| chr7:123601581-123601905 | Rare:66 | ||||
| chr7:123655762-123656234 | Common:2; Rare:131 | ||||
| chr7:123748856-123749258 | Common:3; Rare:143 | ||||
| chr7:124929795-124929999 | Common:3; Rare:65 | ||||
| chr7:127585584-127585682 | Rare:28 | ||||
| chr7:128455663-128455903 | Common:3; Rare:116 | ||||
| chr7:128830581-128830989 | Common:1; Rare:139; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr7:128841175-128841562 | Common:2; Rare:126; Clinvar:13; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr7:129054878-129055226 | Common:2; Rare:66 | ||||
| chr7:129434248-129434467 | Common:1; Rare:80 | ||||
| chr7:129611623-129611755 | Common:1; Rare:39 | ||||
| chr7:131109876-131110029 | Rare:30 | ||||
| chr7:131110046-131110129 | Rare:15 | ||||
| chr7:131327686-131327909 | Rare:67 |