| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26196399-26196557 | Common:1; Rare:70; Clinvar (benign):2 | ||||
| chr7:26200564-26201008 | Common:2; Rare:212 | ||||
| chr7:26201410-26201821 | Common:2; Rare:194 | ||||
| chr7:27095859-27096167 | Rare:84 | ||||
| chr7:27165521-27165591 | Common:1; Rare:31 | ||||
| chr7:27179824-27179894 | Rare:32 | ||||
| chr7:27185185-27185397 | Common:1; Rare:82 | ||||
| chr7:27662789-27663198 | Common:8; Rare:149 | ||||
| chr7:27740037-27740199 | Common:5; Rare:47 | ||||
| chr7:30478681-30478797 | Common:1; Rare:44 | ||||
| chr7:30594722-30594935 | Common:3; Rare:98; Clinvar:6; Clinvar (benign):6 | ||||
| chr7:30771306-30771436 | Common:1; Rare:35 | ||||
| chr7:32495247-32495635 | Common:1; Rare:104 | ||||
| chr7:33129228-33129571 | Common:5; Rare:97 | ||||
| chr7:35800721-35801252 | Common:2; Rare:201 |