| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38663590-38664403 | Common:7; Rare:591 | ||||
| chr4:38664793-38665206 | Common:4; Rare:201 | ||||
| chr4:38867546-38867901 | Common:3; Rare:189 | ||||
| chr4:39044475-39045072 | Common:16; Rare:340 | ||||
| chr4:39182163-39182669 | Common:1; Rare:202; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:39366061-39366501 | Common:5; Rare:232 | ||||
| chr4:39458651-39459170 | Common:13; Rare:579; Clinvar:9; Clinvar (benign):17 | ||||
| chr4:39527286-39528076 | Common:12; Rare:378 | ||||
| chr4:39528120-39528793 | Common:6; Rare:172 | ||||
| chr4:39638072-39638472 | Common:3; Rare:101 | ||||
| chr4:39638572-39639269 | Common:4; Rare:573 | ||||
| chr4:39639512-39640485 | Common:9; Rare:255 | ||||
| chr4:39697339-39697860 | Common:19; Rare:164 | ||||
| chr4:39697788-39698449 | Common:6; Rare:489 | ||||
| chr4:39698660-39699010 | Rare:98 |