| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4290088-4290232 | Common:3; Rare:59 | ||||
| chr4:4541968-4542199 | Common:2; Rare:98 | ||||
| chr4:6640541-6640731 | Common:3; Rare:78 | ||||
| chr4:6709773-6709971 | Rare:60 | ||||
| chr4:6987034-6987296 | Common:1; Rare:83 | ||||
| chr4:7068034-7068385 | Common:6; Rare:120 | ||||
| chr4:10116668-10117113 | Common:10; Rare:216 | ||||
| chr4:15003160-15003203 | Common:1; Rare:17 | ||||
| chr4:15681423-15681756 | Common:3; Rare:104 | ||||
| chr4:15702985-15703134 | Common:1; Rare:30 | ||||
| chr4:17810685-17811028 | Common:3; Rare:105 | ||||
| chr4:25160405-25160727 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233862-25234089 | Rare:99 | ||||
| chr4:26857441-26857753 | Common:4; Rare:84 | ||||
| chr4:26860579-26860865 | Common:3; Rare:99 |