| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:44678390-44678496 | Rare:37 | ||||
| chr4:44678615-44678778 | Rare:72 | ||||
| chr4:44726477-44726644 | Common:2; Rare:58 | ||||
| chr4:48016643-48016806 | Common:1; Rare:51 | ||||
| chr4:48080038-48080327 | Common:2; Rare:69 | ||||
| chr4:48269782-48269981 | Common:2; Rare:47 | ||||
| chr4:48906666-48906902 | Rare:54 | ||||
| chr4:51842819-51843239 | Common:1; Rare:130 | ||||
| chr4:52659161-52659420 | Common:1; Rare:88 | ||||
| chr4:52862173-52862317 | Common:5; Rare:63 | ||||
| chr4:53377565-53377920 | Common:2; Rare:121 | ||||
| chr4:54229216-54229357 | Common:1; Rare:24; Clinvar (benign):2 | ||||
| chr4:55396067-55396391 | Common:1; Rare:99; Clinvar (benign):3 | ||||
| chr4:55546818-55547152 | Common:2; Rare:123 | ||||
| chr4:55853842-55853915 | Rare:7 |