| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17810696-17811012 | Common:2; Rare:98 | ||||
| chr4:25160405-25160727 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233849-25234105 | Rare:104 | ||||
| chr4:25914051-25914266 | Common:2; Rare:95 | ||||
| chr4:26320450-26320818 | Common:1; Rare:110 | ||||
| chr4:26320944-26321051 | Rare:44 | ||||
| chr4:26857438-26857739 | Common:4; Rare:80 | ||||
| chr4:26860603-26860849 | Common:3; Rare:86 | ||||
| chr4:39458830-39459109 | Common:3; Rare:152; Clinvar (benign):5 | ||||
| chr4:39638844-39639159 | Common:1; Rare:115 | ||||
| chr4:39697889-39698195 | Common:2; Rare:126 | ||||
| chr4:39698347-39698385 | Rare:4 | ||||
| chr4:41990406-41990586 | Common:1; Rare:66 | ||||
| chr4:44726489-44726637 | Common:2; Rare:53 | ||||
| chr4:52659267-52659479 | Common:1; Rare:68 |