| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15427889-15428057 | Rare:21 | ||||
| chr4:15478584-15478806 | Common:1; Rare:38; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:15655210-15655491 | Common:2; Rare:107 | ||||
| chr4:15681564-15681893 | Common:4; Rare:118 | ||||
| chr4:15703013-15703049 | Common:1; Rare:9 | ||||
| chr4:15703056-15703147 | Rare:21 | ||||
| chr4:16227578-16227729 | Rare:38 | ||||
| chr4:16898470-16899005 | Common:14; Rare:100 | ||||
| chr4:17512050-17512326 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:17614523-17614651 | Common:2; Rare:50 | ||||
| chr4:17810672-17811017 | Common:3; Rare:109 | ||||
| chr4:18021719-18021780 | Rare:22 | ||||
| chr4:20252794-20253151 | Rare:93 | ||||
| chr4:23890030-23890278 | Common:1; Rare:39 | ||||
| chr4:24584381-24584699 | Rare:102 |