| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30594722-30595001 | Common:4; Rare:134; Clinvar:6; Clinvar (benign):9 | ||||
| chr7:32490294-32490553 | Common:2; Rare:78 | ||||
| chr7:32495247-32495607 | Common:1; Rare:92 | ||||
| chr7:33062677-33062895 | Common:2; Rare:94 | ||||
| chr7:33063122-33063195 | Rare:21 | ||||
| chr7:33109370-33109513 | Rare:52 | ||||
| chr7:33129473-33129564 | Common:1; Rare:25 | ||||
| chr7:35694876-35695245 | Common:3; Rare:104 | ||||
| chr7:35800936-35801264 | Common:2; Rare:139 | ||||
| chr7:37342762-37342861 | Rare:18 | ||||
| chr7:38178005-38178400 | Common:3; Rare:118 | ||||
| chr7:39566306-39566324 | Rare:10 | ||||
| chr7:39566335-39566482 | Common:2; Rare:71 | ||||
| chr7:39623508-39623819 | Rare:99 | ||||
| chr7:39949485-39949653 | Common:1; Rare:57 |