| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23181710-23181856 | Rare:35 | ||||
| chr7:23181912-23182096 | Rare:79 | ||||
| chr7:26196557-26197018 | Common:2; Rare:156; Clinvar (benign):3 | ||||
| chr7:26200571-26200941 | Common:1; Rare:180 | ||||
| chr7:26200978-26201557 | Common:1; Rare:234 | ||||
| chr7:26201586-26201824 | Common:2; Rare:124 | ||||
| chr7:26202844-26202889 | Rare:11 | ||||
| chr7:27096011-27096120 | Rare:33 | ||||
| chr7:27172851-27173062 | Rare:54 | ||||
| chr7:27185183-27185440 | Common:1; Rare:92 | ||||
| chr7:27200104-27200460 | Common:1; Rare:115 | ||||
| chr7:27740069-27740212 | Common:5; Rare:36 | ||||
| chr7:30504767-30505087 | Common:2; Rare:103 | ||||
| chr7:30594716-30595112 | Common:6; Rare:180; Clinvar:10; Clinvar (benign):14 | ||||
| chr7:32071397-32071492 | Common:1; Rare:11 |