| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:86973375-86973430 | Rare:5 | ||||
| chr4:86973454-86973774 | Rare:76 | ||||
| chr4:86979389-86979503 | Rare:21 | ||||
| chr4:86987979-86988180 | Common:2; Rare:47 | ||||
| chr4:87013691-87013730 | Rare:4 | ||||
| chr4:87105632-87105756 | Common:1; Rare:31 | ||||
| chr4:87120865-87121183 | Common:2; Rare:66 | ||||
| chr4:87892489-87892624 | Common:1; Rare:41 | ||||
| chr4:87893504-87893512 | Rare:2 | ||||
| chr4:88046831-88047157 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr4:88415861-88415921 | Rare:2 | ||||
| chr4:88434788-88434899 | Common:1; Rare:15 | ||||
| chr4:88533306-88533395 | Rare:19 | ||||
| chr4:88608954-88609107 | Common:1; Rare:19 | ||||
| chr4:88609861-88610053 | Common:2; Rare:33 |