| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4248198-4248239 | Rare:17 | ||||
| chr4:4290117-4290277 | Common:3; Rare:64 | ||||
| chr4:4541969-4542192 | Common:2; Rare:92 | ||||
| chr4:6640537-6640799 | Common:3; Rare:92 | ||||
| chr4:6693672-6693875 | Rare:38 | ||||
| chr4:6986992-6987310 | Common:2; Rare:103 | ||||
| chr4:7068019-7068359 | Common:6; Rare:110 | ||||
| chr4:8435998-8436113 | Common:1; Rare:18 | ||||
| chr4:8440717-8440834 | Rare:48 | ||||
| chr4:15427942-15428060 | Rare:12 | ||||
| chr4:15655232-15655468 | Common:2; Rare:97 | ||||
| chr4:15681458-15681869 | Common:3; Rare:142 | ||||
| chr4:17614551-17614651 | Common:2; Rare:43 | ||||
| chr4:17810681-17811017 | Common:3; Rare:103 | ||||
| chr4:25160376-25160704 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):1 |