| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132257475-132257744 | Common:8; Rare:72 | ||||
| chr5:132294086-132294439 | Common:1; Rare:84 | ||||
| chr5:132295257-132295481 | Rare:45 | ||||
| chr5:132369580-132369767 | Common:4; Rare:56; Clinvar (benign):1 | ||||
| chr5:132369883-132370162 | Common:2; Rare:112; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):14 | ||||
| chr5:132410603-132410995 | Common:1; Rare:81 | ||||
| chr5:132490717-132491020 | Common:1; Rare:80 | ||||
| chr5:132556803-132557043 | Common:1; Rare:84; Clinvar:1 | ||||
| chr5:132737496-132737650 | Rare:48 | ||||
| chr5:132866457-132866673 | Common:1; Rare:68 | ||||
| chr5:132963286-132963720 | Common:3; Rare:110 | ||||
| chr5:133026524-133026777 | Common:5; Rare:57 | ||||
| chr5:133051851-133052274 | Rare:144 | ||||
| chr5:133968546-133968737 | Rare:79 | ||||
| chr5:134004521-134004861 | Common:1; Rare:118 |