| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:140427652-140427673 | Rare:3 | ||||
| chr4:141636771-141636991 | Common:1; Rare:46 | ||||
| chr4:142405389-142405550 | Rare:24 | ||||
| chr4:143513349-143513507 | Common:2; Rare:53 | ||||
| chr4:145098129-145098354 | Rare:75 | ||||
| chr4:145619084-145619402 | Common:1; Rare:103 | ||||
| chr4:147684127-147684357 | Rare:96 | ||||
| chr4:152779705-152780160 | Common:2; Rare:117 | ||||
| chr4:158671849-158672355 | Common:5; Rare:123; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723335-158723480 | Common:2; Rare:65 | ||||
| chr4:165327383-165327741 | Common:3; Rare:107 | ||||
| chr4:169010227-169010362 | Common:1; Rare:47 | ||||
| chr4:173530205-173530462 | Common:2; Rare:59 | ||||
| chr4:174283612-174283976 | Common:1; Rare:74 | ||||
| chr4:177442377-177442529 | Rare:91; Clinvar:2 |