| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39697936-39698192 | Common:2; Rare:109 | ||||
| chr4:40056650-40056907 | Common:4; Rare:79 | ||||
| chr4:41360670-41360875 | Common:1; Rare:53 | ||||
| chr4:41990331-41990590 | Common:1; Rare:84 | ||||
| chr4:44678390-44678706 | Common:1; Rare:118 | ||||
| chr4:44726523-44726622 | Rare:41 | ||||
| chr4:46993431-46993664 | Common:2; Rare:59 | ||||
| chr4:46994296-46994359 | Common:1; Rare:12 | ||||
| chr4:47485191-47485363 | Common:1; Rare:61 | ||||
| chr4:47837472-47837526 | Rare:5 | ||||
| chr4:48269822-48270030 | Common:1; Rare:43 | ||||
| chr4:48341286-48341581 | Common:1; Rare:124 | ||||
| chr4:48341771-48341978 | Rare:61 | ||||
| chr4:48780197-48780626 | Common:3; Rare:133 | ||||
| chr4:52038230-52038329 | Rare:45; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 |