| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:127651876-127652260 | Common:2; Rare:115 | ||||
| chr7:128409883-128410085 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455736-128455919 | Common:2; Rare:106 | ||||
| chr7:128739202-128739427 | Common:1; Rare:59 | ||||
| chr7:128830582-128830779 | Rare:72; Clinvar:6; Clinvar (benign):4 | ||||
| chr7:128830909-128830988 | Rare:21; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:129054878-129055234 | Common:2; Rare:67 | ||||
| chr7:129434268-129434452 | Common:1; Rare:65 | ||||
| chr7:129611607-129611784 | Common:2; Rare:59 | ||||
| chr7:130205380-130205559 | Rare:78 | ||||
| chr7:131109896-131110136 | Common:1; Rare:41 | ||||
| chr7:131327688-131327909 | Rare:67 | ||||
| chr7:133252876-133253156 | Rare:97 | ||||
| chr7:134316829-134317175 | Common:2; Rare:99 | ||||
| chr7:134646577-134646864 | Common:6; Rare:85 |