| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23105682-23105841 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181959-23182128 | Rare:72 | ||||
| chr7:23299193-23299378 | Common:2; Rare:93 | ||||
| chr7:23470362-23470560 | Rare:58 | ||||
| chr7:23531948-23532085 | Common:1; Rare:54 | ||||
| chr7:25125251-25125604 | Rare:141; Clinvar:3 | ||||
| chr7:26200549-26201013 | Common:2; Rare:226 | ||||
| chr7:26201025-26201284 | Common:1; Rare:109 | ||||
| chr7:26201323-26201560 | Rare:84 | ||||
| chr7:26201574-26201800 | Common:2; Rare:121 | ||||
| chr7:26864558-26864840 | Common:3; Rare:85 | ||||
| chr7:27095974-27096199 | Rare:67 | ||||
| chr7:27152547-27152744 | Rare:35 | ||||
| chr7:27172795-27173074 | Rare:66 | ||||
| chr7:27179836-27179912 | Rare:32 |