| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:130205371-130205498 | Rare:63 | ||||
| chr7:130440977-130441274 | Common:3; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:130491965-130492339 | Common:1; Rare:99 | ||||
| chr7:131109834-131110156 | Common:1; Rare:59 | ||||
| chr7:131327686-131327912 | Rare:69 | ||||
| chr7:134316723-134317175 | Common:2; Rare:125 | ||||
| chr7:134458999-134459216 | Common:3; Rare:100 | ||||
| chr7:134459227-134459297 | Common:1; Rare:24 | ||||
| chr7:134646569-134646893 | Common:6; Rare:105 | ||||
| chr7:134779365-134779775 | Common:2; Rare:66 | ||||
| chr7:134986473-134986556 | Common:3; Rare:38 | ||||
| chr7:135147991-135148239 | Rare:52 | ||||
| chr7:135170393-135170993 | Common:7; Rare:198 | ||||
| chr7:135662389-135662556 | Common:3; Rare:80 | ||||
| chr7:138460858-138461106 | Common:1; Rare:80 |