| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134779776-134779833 | Rare:6 | ||||
| chr7:134780121-134780266 | Rare:23 | ||||
| chr7:134965086-134965406 | Common:1; Rare:81 | ||||
| chr7:134986629-134986670 | Rare:6 | ||||
| chr7:135148023-135148137 | Rare:31 | ||||
| chr7:135170452-135170821 | Common:3; Rare:136 | ||||
| chr7:135211476-135211729 | Common:2; Rare:125 | ||||
| chr7:135662357-135662543 | Common:4; Rare:81 | ||||
| chr7:136868591-136868852 | Common:1; Rare:56 | ||||
| chr7:136869072-136869312 | Common:2; Rare:52; Clinvar (benign):3 | ||||
| chr7:139109337-139109492 | Common:1; Rare:46 | ||||
| chr7:139109696-139109929 | Common:2; Rare:58 | ||||
| chr7:139133675-139133828 | Rare:40 | ||||
| chr7:139341262-139341419 | Common:1; Rare:49 | ||||
| chr7:139359350-139359528 | Common:1; Rare:67 |