| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139359677-139360008 | Common:3; Rare:129 | ||||
| chr7:140479357-140479404 | Rare:11 | ||||
| chr7:141551342-141551420 | Rare:22; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:142854990-142855133 | Common:2; Rare:42 | ||||
| chr7:143380931-143381040 | Rare:28 | ||||
| chr7:148698596-148699000 | Common:3; Rare:143 | ||||
| chr7:150323493-150323668 | Rare:59 | ||||
| chr7:150379061-150379355 | Common:2; Rare:105 | ||||
| chr7:151028149-151028440 | Rare:88 | ||||
| chr7:151080786-151080972 | Rare:58 | ||||
| chr7:152025574-152025745 | Rare:69 | ||||
| chr7:155644377-155644718 | Common:2; Rare:117 | ||||
| chr7:157010647-157010926 | Common:3; Rare:81 | ||||
| chr7:157336790-157337075 | Common:2; Rare:133; Clinvar:1 | ||||
| chr8:232181-232397 | Common:3; Rare:80 |