| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:133149088-133149389 | Common:2; Rare:88 | ||||
| chr4:139084190-139084439 | Common:2; Rare:101 | ||||
| chr4:139301199-139301584 | Common:6; Rare:113 | ||||
| chr4:139453774-139454204 | Common:3; Rare:112; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373384-140373701 | Common:2; Rare:129 | ||||
| chr4:140523987-140524252 | Common:1; Rare:78 | ||||
| chr4:141636770-141636900 | Common:1; Rare:31 | ||||
| chr4:143184859-143184963 | Common:3; Rare:42 | ||||
| chr4:143513642-143513789 | Rare:50 | ||||
| chr4:144645931-144646168 | Common:1; Rare:64 | ||||
| chr4:145098138-145098404 | Rare:87 | ||||
| chr4:145619273-145619402 | Rare:56 | ||||
| chr4:145938382-145938694 | Common:2; Rare:62 | ||||
| chr4:147617213-147617499 | Common:1; Rare:65 | ||||
| chr4:147684118-147684265 | Common:1; Rare:56 |