| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128405910-128406118 | Common:2; Rare:74 | ||||
| chr7:128409851-128410081 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455663-128455903 | Common:3; Rare:116 | ||||
| chr7:128476645-128476840 | Common:1; Rare:75 | ||||
| chr7:128739152-128739427 | Common:2; Rare:73 | ||||
| chr7:128791316-128791496 | Rare:46 | ||||
| chr7:128830524-128830553 | Rare:3 | ||||
| chr7:128830581-128830989 | Common:1; Rare:139; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr7:128840949-128841178 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):6 | ||||
| chr7:129054878-129055226 | Common:2; Rare:66 | ||||
| chr7:129611616-129611803 | Common:1; Rare:59 | ||||
| chr7:130051359-130051447 | Rare:34 | ||||
| chr7:131109828-131110146 | Common:1; Rare:60 | ||||
| chr7:131327686-131327909 | Rare:67 | ||||
| chr7:134646582-134646856 | Common:6; Rare:77 |