| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38867508-38867830 | Common:2; Rare:95 | ||||
| chr4:39366245-39366403 | Common:1; Rare:50 | ||||
| chr4:39454685-39454938 | Common:2; Rare:64 | ||||
| chr4:39454964-39455059 | Common:1; Rare:31 | ||||
| chr4:39458833-39459112 | Common:3; Rare:153; Clinvar (benign):5 | ||||
| chr4:39527359-39527754 | Common:2; Rare:93 | ||||
| chr4:39527916-39528006 | Rare:22 | ||||
| chr4:39638832-39639155 | Common:1; Rare:118 | ||||
| chr4:39697973-39698243 | Common:1; Rare:105 | ||||
| chr4:39698331-39698386 | Rare:5 | ||||
| chr4:39848495-39848699 | Rare:25 | ||||
| chr4:41256811-41257008 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41261871-41261953 | Rare:29 | ||||
| chr4:41990412-41990758 | Common:3; Rare:128 | ||||
| chr4:44678624-44678733 | Rare:51 |