| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:663616-663748 | Rare:44 | ||||
| chr4:673814-673913 | Common:1; Rare:34 | ||||
| chr4:674212-674558 | Common:2; Rare:159 | ||||
| chr4:681111-681227 | Rare:44 | ||||
| chr4:705562-705949 | Common:1; Rare:131 | ||||
| chr4:932259-932487 | Common:2; Rare:88 | ||||
| chr4:986904-987176 | Common:3; Rare:94; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113533-1113642 | Common:1; Rare:43 | ||||
| chr4:1720535-1720608 | Rare:16 | ||||
| chr4:1974396-1974635 | Common:1; Rare:52 | ||||
| chr4:2468878-2469159 | Common:3; Rare:101 | ||||
| chr4:2843667-2844016 | Common:3; Rare:126 | ||||
| chr4:2934777-2934910 | Common:1; Rare:64 | ||||
| chr4:2963328-2963898 | Common:4; Rare:168 | ||||
| chr4:3074536-3074698 | Common:3; Rare:49 |