| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:86849367-86849496 | Common:2; Rare:23 | ||||
| chr4:86934860-86935208 | Common:3; Rare:130 | ||||
| chr4:86936162-86936466 | Common:2; Rare:67 | ||||
| chr4:87006876-87007250 | Common:4; Rare:97 | ||||
| chr4:87422524-87422653 | Common:1; Rare:36 | ||||
| chr4:87529059-87529422 | Common:2; Rare:60 | ||||
| chr4:88284690-88284938 | Common:2; Rare:67 | ||||
| chr4:88523598-88523856 | Common:2; Rare:89 | ||||
| chr4:88592299-88592569 | Common:1; Rare:82 | ||||
| chr4:88593151-88593371 | Common:3; Rare:45 | ||||
| chr4:88697816-88697870 | Rare:19 | ||||
| chr4:88823089-88823433 | Common:4; Rare:67 | ||||
| chr4:89111097-89111187 | Rare:17 | ||||
| chr4:89111347-89111635 | Common:4; Rare:103 | ||||
| chr4:89836975-89837292 | Common:4; Rare:109; Clinvar:4; Clinvar (benign):1 |