| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139453774-139454219 | Common:3; Rare:121; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556123-139556519 | Rare:82 | ||||
| chr4:140257091-140257322 | Common:3; Rare:36 | ||||
| chr4:140373380-140373709 | Common:3; Rare:133 | ||||
| chr4:143184710-143184914 | Common:8; Rare:79 | ||||
| chr4:144645927-144646170 | Common:1; Rare:67 | ||||
| chr4:144646321-144646824 | Common:1; Rare:115 | ||||
| chr4:145098126-145098350 | Rare:74 | ||||
| chr4:145482488-145482821 | Common:2; Rare:90 | ||||
| chr4:145482942-145483001 | Rare:5 | ||||
| chr4:145619353-145619402 | Rare:16 | ||||
| chr4:148442412-148442713 | Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:151015722-151015844 | Rare:58 | ||||
| chr4:152679901-152680120 | Rare:69 | ||||
| chr4:152779796-152780009 | Common:1; Rare:57 |