| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:128287465-128287576 | Common:1; Rare:44 | ||||
| chr4:128287705-128288029 | Common:3; Rare:126 | ||||
| chr4:128809605-128809787 | Rare:52 | ||||
| chr4:133149097-133149323 | Common:2; Rare:70 | ||||
| chr4:137531874-137532082 | Rare:57 | ||||
| chr4:139301281-139301538 | Common:4; Rare:78 | ||||
| chr4:140373358-140373710 | Common:3; Rare:141 | ||||
| chr4:143513617-143513922 | Common:1; Rare:108 | ||||
| chr4:145098146-145098367 | Rare:78 | ||||
| chr4:145619306-145619394 | Rare:40 | ||||
| chr4:147617213-147617491 | Common:1; Rare:62 | ||||
| chr4:151226356-151226524 | Rare:28 | ||||
| chr4:152679935-152680114 | Rare:41 | ||||
| chr4:152779653-152780220 | Common:3; Rare:146 | ||||
| chr4:158671809-158672325 | Common:5; Rare:132; Clinvar:2; Clinvar (benign):1 |