| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:30721978-30722182 | Common:1; Rare:63 | ||||
| chr4:37826571-37826748 | Common:1; Rare:67 | ||||
| chr4:37977189-37977447 | Rare:65 | ||||
| chr4:38867588-38867826 | Common:2; Rare:84 | ||||
| chr4:38867976-38868115 | Common:1; Rare:38 | ||||
| chr4:39182227-39182548 | Rare:71; Clinvar:2 | ||||
| chr4:39458864-39459122 | Common:3; Rare:146; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527314-39527761 | Common:6; Rare:113 | ||||
| chr4:39527959-39528021 | Rare:13 | ||||
| chr4:39638829-39639154 | Common:1; Rare:119 | ||||
| chr4:39697936-39698203 | Common:2; Rare:116 | ||||
| chr4:41990402-41990580 | Common:1; Rare:65 | ||||
| chr4:44678209-44678706 | Common:3; Rare:168 | ||||
| chr4:44726481-44726635 | Common:2; Rare:54 | ||||
| chr4:47485214-47485397 | Common:2; Rare:61 |