| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:40630243-40630272 | Common:1; Rare:6 | ||||
| chr4:40749826-40750007 | Common:1; Rare:52 | ||||
| chr4:41256713-41257133 | Common:5; Rare:137; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:41261711-41261922 | Rare:78; Clinvar:1 | ||||
| chr4:41359518-41359614 | Rare:16 | ||||
| chr4:41360715-41360801 | Common:1; Rare:26 | ||||
| chr4:41612879-41612940 | Rare:8 | ||||
| chr4:41935004-41935527 | Common:4; Rare:151 | ||||
| chr4:41990357-41990742 | Common:3; Rare:138 | ||||
| chr4:42657043-42657349 | Common:5; Rare:116 | ||||
| chr4:44448915-44449150 | Common:1; Rare:72 | ||||
| chr4:44678360-44678732 | Common:1; Rare:139 | ||||
| chr4:44726547-44726657 | Rare:47 | ||||
| chr4:47463602-47463817 | Common:2; Rare:85 | ||||
| chr4:47485191-47485365 | Common:1; Rare:61 |