| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38867570-38867822 | Common:2; Rare:86 | ||||
| chr4:38868312-38868471 | Common:1; Rare:32 | ||||
| chr4:39366319-39366431 | Rare:35 | ||||
| chr4:39458857-39459122 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527383-39527742 | Common:2; Rare:87 | ||||
| chr4:39527961-39528016 | Rare:13 | ||||
| chr4:39638834-39639186 | Common:1; Rare:132 | ||||
| chr4:39697936-39698203 | Common:2; Rare:116 | ||||
| chr4:39977339-39977636 | Common:2; Rare:84 | ||||
| chr4:41214425-41214742 | Common:5; Rare:81 | ||||
| chr4:41990380-41990586 | Common:1; Rare:75 | ||||
| chr4:44678382-44678724 | Common:1; Rare:131 | ||||
| chr4:44726487-44726659 | Common:2; Rare:64 | ||||
| chr4:47463621-47463774 | Common:1; Rare:57 | ||||
| chr4:47485211-47485340 | Common:1; Rare:48 |