| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134646563-134646873 | Common:6; Rare:94 | ||||
| chr7:135148000-135148109 | Rare:27 | ||||
| chr7:135170627-135170989 | Common:6; Rare:120 | ||||
| chr7:135662357-135662543 | Common:4; Rare:81 | ||||
| chr7:135977305-135977530 | Common:2; Rare:86 | ||||
| chr7:139036023-139036224 | Rare:54 | ||||
| chr7:139109327-139109495 | Common:1; Rare:50 | ||||
| chr7:139109716-139109825 | Common:1; Rare:28 | ||||
| chr7:139341245-139341380 | Rare:30 | ||||
| chr7:139359677-139359974 | Common:2; Rare:120 | ||||
| chr7:140479350-140479454 | Rare:27 | ||||
| chr7:140696597-140696761 | Common:1; Rare:60 | ||||
| chr7:141014915-141015068 | Rare:34 | ||||
| chr7:141551200-141551428 | Common:3; Rare:59; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738013-141738534 | Common:4; Rare:152 |