| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39697929-39698340 | Common:2; Rare:156 | ||||
| chr4:40056645-40056998 | Common:4; Rare:105 | ||||
| chr4:41214433-41214752 | Common:5; Rare:81 | ||||
| chr4:41256728-41257001 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41261724-41261922 | Rare:76; Clinvar:1 | ||||
| chr4:41360670-41360837 | Common:1; Rare:45 | ||||
| chr4:41612461-41612772 | Rare:67 | ||||
| chr4:41935000-41935200 | Common:3; Rare:57 | ||||
| chr4:41990388-41990623 | Common:1; Rare:82 | ||||
| chr4:42656915-42657209 | Common:7; Rare:103 | ||||
| chr4:44678382-44678472 | Rare:28 | ||||
| chr4:44678624-44678731 | Rare:50 | ||||
| chr4:44726481-44726657 | Common:2; Rare:65 | ||||
| chr4:46123954-46124192 | Common:3; Rare:47 | ||||
| chr4:46993455-46993614 | Rare:41 |