| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:148074828-148075102 | Common:3; Rare:61 | ||||
| chr4:148192278-148192369 | Rare:18 | ||||
| chr4:148251072-148251305 | Common:1; Rare:50 | ||||
| chr4:148445292-148445611 | Common:2; Rare:98 | ||||
| chr4:151135115-151135347 | Rare:41 | ||||
| chr4:151167131-151167164 | Rare:3 | ||||
| chr4:151223809-151223890 | Common:2; Rare:6 | ||||
| chr4:153684039-153684344 | Common:2; Rare:87 | ||||
| chr4:158171485-158171851 | Rare:51 | ||||
| chr4:158706005-158706341 | Rare:88; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr4:158713127-158713463 | Rare:77 | ||||
| chr4:168095995-168096027 | Rare:1 | ||||
| chr4:168097671-168097796 | Common:2; Rare:16 | ||||
| chr4:168098255-168098266 | Rare:1 | ||||
| chr4:168143509-168143793 | Common:1; Rare:52 |