| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:124929795-124929935 | Common:3; Rare:47 | ||||
| chr7:127588236-127588443 | Rare:77 | ||||
| chr7:127651833-127652235 | Common:3; Rare:119 | ||||
| chr7:128455663-128455919 | Common:3; Rare:129 | ||||
| chr7:128476645-128476811 | Common:1; Rare:62 | ||||
| chr7:128830185-128830409 | Common:2; Rare:60 | ||||
| chr7:128830563-128830695 | Rare:56; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:128830905-128830988 | Rare:21; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:129054884-129055234 | Common:2; Rare:67 | ||||
| chr7:129434338-129434460 | Common:1; Rare:52 | ||||
| chr7:129611616-129611783 | Common:1; Rare:54 | ||||
| chr7:130205399-130205520 | Rare:53 | ||||
| chr7:130491965-130492301 | Common:1; Rare:87 | ||||
| chr7:131327704-131327899 | Rare:65 | ||||
| chr7:134646566-134646881 | Common:6; Rare:97 |