| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132294123-132294208 | Rare:17 | ||||
| chr5:132369575-132369760 | Common:3; Rare:57 | ||||
| chr5:132369874-132369936 | Common:2; Rare:21; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:132370147-132370186 | Rare:15; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr5:132410603-132411017 | Common:1; Rare:86 | ||||
| chr5:132490754-132491020 | Rare:68 | ||||
| chr5:132556852-132557020 | Common:1; Rare:64; Clinvar:1 | ||||
| chr5:132777154-132777446 | Common:3; Rare:72 | ||||
| chr5:132830610-132830775 | Rare:46 | ||||
| chr5:132866457-132866716 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963260-132963746 | Common:3; Rare:127 | ||||
| chr5:132963909-132964038 | Rare:50 | ||||
| chr5:133051851-133052351 | Common:1; Rare:161 | ||||
| chr5:133968524-133968707 | Rare:81 | ||||
| chr5:134004508-134005016 | Common:2; Rare:160 |