| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:38178005-38178400 | Common:3; Rare:118 | ||||
| chr7:38631355-38631636 | Common:1; Rare:86 | ||||
| chr7:39566351-39566473 | Common:1; Rare:60 | ||||
| chr7:39622935-39623007 | Rare:18 | ||||
| chr7:39623492-39623819 | Rare:101 | ||||
| chr7:39949436-39949830 | Common:6; Rare:146 | ||||
| chr7:39949929-39950267 | Common:1; Rare:99 | ||||
| chr7:39951559-39951794 | Common:1; Rare:101; Clinvar (benign):1 | ||||
| chr7:40134420-40134517 | Rare:47 | ||||
| chr7:40134581-40134697 | Rare:41 | ||||
| chr7:40134910-40135035 | Rare:39; Clinvar:1 | ||||
| chr7:41700585-41700658 | Rare:11 | ||||
| chr7:42227776-42227984 | Rare:44 | ||||
| chr7:42237299-42237621 | Common:2; Rare:99 | ||||
| chr7:42932105-42932467 | Rare:140 |