| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139453653-139453718 | Common:1; Rare:24 | ||||
| chr4:139453774-139454210 | Common:3; Rare:117; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556403-139556611 | Rare:31 | ||||
| chr4:140373384-140373701 | Common:2; Rare:129 | ||||
| chr4:141220782-141220971 | Rare:62 | ||||
| chr4:141636513-141636633 | Rare:24 | ||||
| chr4:141636771-141636890 | Common:1; Rare:31 | ||||
| chr4:142405423-142405554 | Rare:18 | ||||
| chr4:143184843-143184914 | Common:5; Rare:29 | ||||
| chr4:143513349-143513529 | Common:2; Rare:64 | ||||
| chr4:143513661-143514036 | Common:1; Rare:155 | ||||
| chr4:144645850-144646166 | Common:1; Rare:93 | ||||
| chr4:145098117-145098348 | Rare:74 | ||||
| chr4:145619250-145619406 | Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147480998-147481321 | Common:4; Rare:67 |