| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37826543-37826808 | Common:6; Rare:95 | ||||
| chr4:39182187-39182557 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366245-39366403 | Common:1; Rare:50 | ||||
| chr4:39458829-39459112 | Common:3; Rare:154; Clinvar (benign):5 | ||||
| chr4:39527359-39527756 | Common:2; Rare:94 | ||||
| chr4:39527952-39527984 | Rare:9 | ||||
| chr4:39638844-39639163 | Common:1; Rare:116 | ||||
| chr4:39697780-39698386 | Common:2; Rare:189 | ||||
| chr4:40056761-40056945 | Common:2; Rare:58 | ||||
| chr4:41256725-41256847 | Common:1; Rare:29 | ||||
| chr4:41256849-41257126 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41261711-41261941 | Rare:86; Clinvar:1 | ||||
| chr4:41748824-41749130 | Rare:54 | ||||
| chr4:41934935-41935203 | Common:3; Rare:72 | ||||
| chr4:41990398-41990758 | Common:3; Rare:132 |