| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128791323-128791502 | Rare:45 | ||||
| chr7:128830235-128830506 | Common:4; Rare:74 | ||||
| chr7:128830570-128830989 | Common:1; Rare:140; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr7:129055089-129055265 | Common:1; Rare:37 | ||||
| chr7:129611623-129611803 | Common:1; Rare:57 | ||||
| chr7:130205379-130205520 | Rare:64 | ||||
| chr7:131109857-131110101 | Common:1; Rare:43 | ||||
| chr7:131327651-131327909 | Rare:74 | ||||
| chr7:133081876-133081912 | Rare:9 | ||||
| chr7:134646576-134646922 | Common:8; Rare:110 | ||||
| chr7:134779402-134779747 | Rare:57 | ||||
| chr7:134986446-134986668 | Common:5; Rare:73 | ||||
| chr7:135148001-135148116 | Rare:30 | ||||
| chr7:135170466-135170826 | Common:3; Rare:130 | ||||
| chr7:135662403-135662543 | Common:2; Rare:64 |