| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38664194-38664354 | Common:2; Rare:51 | ||||
| chr4:38664819-38665022 | Rare:67 | ||||
| chr4:39182202-39182548 | Rare:75; Clinvar:2 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39527341-39527987 | Common:4; Rare:166 | ||||
| chr4:39638777-39639169 | Common:1; Rare:137 | ||||
| chr4:39698004-39698185 | Common:1; Rare:74 | ||||
| chr4:40056673-40056971 | Common:4; Rare:98 | ||||
| chr4:41214454-41214701 | Common:5; Rare:61 | ||||
| chr4:41256725-41257020 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41261711-41261949 | Rare:89; Clinvar:1 | ||||
| chr4:41360638-41360843 | Common:2; Rare:56 | ||||
| chr4:41612676-41612930 | Common:1; Rare:44 | ||||
| chr4:41990389-41990626 | Common:1; Rare:82 | ||||
| chr4:44678352-44678505 | Rare:51 |