| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55948743-55948970 | Common:1; Rare:43 | ||||
| chr4:56387014-56387238 | Rare:47 | ||||
| chr4:56387395-56387574 | Rare:66 | ||||
| chr4:56435457-56435974 | Common:6; Rare:170 | ||||
| chr4:56436041-56436331 | Rare:104 | ||||
| chr4:56467422-56467743 | Common:2; Rare:115; Clinvar (benign):5 | ||||
| chr4:56977359-56977751 | Common:3; Rare:145 | ||||
| chr4:57009123-57009661 | Common:5; Rare:87 | ||||
| chr4:57023500-57023752 | Common:1; Rare:40 | ||||
| chr4:67701044-67701449 | Common:4; Rare:182 | ||||
| chr4:70688645-70689091 | Common:2; Rare:127 | ||||
| chr4:70704590-70704782 | Common:1; Rare:64 | ||||
| chr4:70722263-70722403 | Common:2; Rare:21 | ||||
| chr4:70839240-70839387 | Common:2; Rare:56 | ||||
| chr4:70839615-70839690 | Rare:23 |