| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26201361-26201555 | Rare:74 | ||||
| chr7:26201570-26201843 | Common:2; Rare:136 | ||||
| chr7:26864551-26864829 | Common:3; Rare:84 | ||||
| chr7:27095974-27096198 | Rare:66 | ||||
| chr7:27662772-27663160 | Common:6; Rare:135 | ||||
| chr7:27740037-27740212 | Common:5; Rare:52 | ||||
| chr7:28685952-28686148 | Rare:49 | ||||
| chr7:29563661-29563865 | Common:1; Rare:53 | ||||
| chr7:30478676-30478940 | Common:5; Rare:93; Clinvar:1 | ||||
| chr7:30504754-30505085 | Common:2; Rare:110 | ||||
| chr7:30594709-30594950 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):7 | ||||
| chr7:30771306-30771503 | Common:1; Rare:72 | ||||
| chr7:32495238-32495564 | Rare:83 | ||||
| chr7:33062704-33062906 | Common:3; Rare:88 | ||||
| chr7:33129137-33129597 | Common:6; Rare:120 |