| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:124929892-124929962 | Common:1; Rare:26 | ||||
| chr7:127651842-127652216 | Common:3; Rare:106 | ||||
| chr7:128409942-128410261 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455703-128455903 | Common:3; Rare:107 | ||||
| chr7:129054884-129055225 | Common:1; Rare:66 | ||||
| chr7:129611616-129611813 | Common:1; Rare:61 | ||||
| chr7:130205393-130205507 | Rare:50 | ||||
| chr7:131327723-131327902 | Rare:61 | ||||
| chr7:139133654-139133823 | Rare:40 | ||||
| chr7:139341258-139341379 | Rare:29 | ||||
| chr7:141551291-141551423 | Rare:42; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738021-141738423 | Common:4; Rare:122 | ||||
| chr7:143902118-143902292 | Common:5; Rare:55 | ||||
| chr7:149028453-149028769 | Common:7; Rare:122 | ||||
| chr7:149126278-149126438 | Common:5; Rare:51 |