| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38663724-38664296 | Common:3; Rare:272 | ||||
| chr4:38664740-38664911 | Common:1; Rare:57 | ||||
| chr4:38867588-38867846 | Common:4; Rare:172 | ||||
| chr4:38868070-38868640 | Common:2; Rare:206 | ||||
| chr4:39044497-39045072 | Common:16; Rare:291 | ||||
| chr4:39182174-39182563 | Common:2; Rare:173; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:39366289-39366443 | Common:2; Rare:87 | ||||
| chr4:39406950-39407300 | Common:4; Rare:182 | ||||
| chr4:39458591-39459122 | Common:9; Rare:375; Clinvar:2; Clinvar (benign):10 | ||||
| chr4:39527280-39527784 | Common:12; Rare:260 | ||||
| chr4:39527944-39528065 | Rare:53 | ||||
| chr4:39638823-39639206 | Common:2; Rare:260 | ||||
| chr4:39697876-39698279 | Common:4; Rare:285 | ||||
| chr4:39977338-39977708 | Common:6; Rare:201 | ||||
| chr4:39977786-39978053 | Common:4; Rare:148 |