| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:136868561-136868865 | Common:1; Rare:68 | ||||
| chr7:136868970-136869288 | Common:2; Rare:65; Clinvar (benign):3 | ||||
| chr7:137513521-137513824 | Rare:61 | ||||
| chr7:137513990-137514004 | Rare:2 | ||||
| chr7:139109327-139109433 | Common:1; Rare:32 | ||||
| chr7:139340386-139340503 | Rare:32 | ||||
| chr7:139359478-139359535 | Rare:18 | ||||
| chr7:139359692-139360008 | Common:3; Rare:122 | ||||
| chr7:140641458-140641644 | Rare:34 | ||||
| chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738013-141738464 | Common:4; Rare:137 | ||||
| chr7:142854998-142855133 | Common:2; Rare:41 | ||||
| chr7:143263392-143263523 | Rare:40 | ||||
| chr7:143288051-143288442 | Common:2; Rare:133 | ||||
| chr7:143380886-143381397 | Common:2; Rare:158 |