| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25376955-25377325 | Common:4; Rare:110 | ||||
| chr4:25914051-25914316 | Common:2; Rare:114 | ||||
| chr4:26320905-26321046 | Rare:51; Clinvar (benign):1 | ||||
| chr4:37826488-37826744 | Common:7; Rare:90 | ||||
| chr4:37977168-37977447 | Rare:68 | ||||
| chr4:38867674-38867822 | Common:1; Rare:59 | ||||
| chr4:39366324-39366416 | Rare:29 | ||||
| chr4:39458843-39459112 | Common:3; Rare:152; Clinvar (benign):5 | ||||
| chr4:39527383-39527735 | Common:2; Rare:83 | ||||
| chr4:39638847-39639165 | Common:1; Rare:116 | ||||
| chr4:39697936-39698185 | Common:2; Rare:108 | ||||
| chr4:41990389-41990586 | Common:1; Rare:71 | ||||
| chr4:44678338-44678496 | Common:1; Rare:52 | ||||
| chr4:44678608-44678742 | Rare:63 | ||||
| chr4:48016634-48016776 | Common:1; Rare:40 |