| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2843678-2844005 | Common:3; Rare:121 | ||||
| chr4:2934768-2934910 | Common:1; Rare:66 | ||||
| chr4:4248187-4248293 | Common:2; Rare:46 | ||||
| chr4:4290038-4290287 | Common:5; Rare:93 | ||||
| chr4:4541970-4542096 | Common:1; Rare:60 | ||||
| chr4:6640549-6640737 | Common:3; Rare:76 | ||||
| chr4:6709815-6709974 | Rare:48 | ||||
| chr4:6987006-6987288 | Common:2; Rare:88 | ||||
| chr4:7068021-7068347 | Common:5; Rare:108 | ||||
| chr4:8440717-8441009 | Rare:112 | ||||
| chr4:15681447-15681875 | Common:4; Rare:148 | ||||
| chr4:17614548-17614650 | Common:2; Rare:43 | ||||
| chr4:17810687-17811080 | Common:4; Rare:122 | ||||
| chr4:25160413-25160710 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25233989 | Rare:57 |