| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39182227-39182548 | Rare:71; Clinvar:2 | ||||
| chr4:39458868-39459112 | Common:3; Rare:136; Clinvar (benign):5 | ||||
| chr4:39527337-39527755 | Common:4; Rare:104 | ||||
| chr4:39527943-39527987 | Rare:9 | ||||
| chr4:39638834-39639149 | Common:1; Rare:115 | ||||
| chr4:39697936-39698222 | Common:2; Rare:123 | ||||
| chr4:40056677-40056930 | Common:4; Rare:88 | ||||
| chr4:41360611-41360837 | Common:2; Rare:65 | ||||
| chr4:41990389-41990607 | Common:1; Rare:75 | ||||
| chr4:44678390-44678477 | Rare:26 | ||||
| chr4:44678615-44678731 | Rare:55 | ||||
| chr4:44726484-44726537 | Common:2; Rare:13 | ||||
| chr4:44726547-44726657 | Rare:47 | ||||
| chr4:47485191-47485359 | Common:1; Rare:61 | ||||
| chr4:47837469-47837530 | Rare:7 |