| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:40056662-40056992 | Common:4; Rare:102 | ||||
| chr4:41214440-41214764 | Common:5; Rare:80 | ||||
| chr4:41256728-41257000 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41360693-41360819 | Common:1; Rare:39 | ||||
| chr4:41935073-41935187 | Common:2; Rare:30 | ||||
| chr4:41990428-41990576 | Common:1; Rare:56 | ||||
| chr4:44678382-44678448 | Rare:22 | ||||
| chr4:44678593-44678706 | Rare:52 | ||||
| chr4:44726516-44726644 | Rare:47 | ||||
| chr4:46123978-46124192 | Common:3; Rare:40 | ||||
| chr4:46993436-46993895 | Common:2; Rare:113 | ||||
| chr4:47485219-47485355 | Common:1; Rare:50 | ||||
| chr4:47914520-47914843 | Common:1; Rare:99 | ||||
| chr4:48016624-48016784 | Common:1; Rare:47 | ||||
| chr4:48341192-48341483 | Common:1; Rare:121 |