| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128937783-128937982 | Common:2; Rare:34 | ||||
| chr7:129054768-129055231 | Common:2; Rare:106; Clinvar (benign):2 | ||||
| chr7:129434248-129434452 | Common:1; Rare:72 | ||||
| chr7:129611616-129611781 | Common:1; Rare:53 | ||||
| chr7:130205371-130205533 | Rare:78 | ||||
| chr7:130490967-130491121 | Common:1; Rare:35 | ||||
| chr7:131109820-131110136 | Common:1; Rare:60 | ||||
| chr7:131327677-131327909 | Rare:71 | ||||
| chr7:131505904-131506198 | Common:2; Rare:91 | ||||
| chr7:132576449-132576609 | Common:2; Rare:40 | ||||
| chr7:134459053-134459311 | Common:4; Rare:108 | ||||
| chr7:134646566-134646856 | Common:6; Rare:83 | ||||
| chr7:134986340-134986676 | Common:7; Rare:107 | ||||
| chr7:135148028-135148190 | Rare:39 | ||||
| chr7:135170627-135170841 | Common:2; Rare:84 |