| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132490750-132491026 | Rare:70 | ||||
| chr5:132556813-132557045 | Common:1; Rare:80; Clinvar:1 | ||||
| chr5:132777140-132777360 | Common:3; Rare:53 | ||||
| chr5:132830623-132830770 | Rare:43 | ||||
| chr5:132866457-132866690 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963489-132963825 | Common:1; Rare:83 | ||||
| chr5:133051862-133052216 | Rare:119 | ||||
| chr5:133968560-133968744 | Rare:76 | ||||
| chr5:134004516-134004861 | Common:2; Rare:120 | ||||
| chr5:134004894-134005016 | Rare:27 | ||||
| chr5:134176835-134177067 | Common:4; Rare:92 | ||||
| chr5:134225552-134225609 | Common:1; Rare:22 | ||||
| chr5:134225995-134226413 | Common:1; Rare:135 | ||||
| chr5:134371027-134371637 | Common:5; Rare:202 | ||||
| chr5:134411846-134412009 | Rare:56 |