| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132737485-132737661 | Rare:58 | ||||
| chr5:132777138-132777347 | Common:3; Rare:49 | ||||
| chr5:132830617-132830759 | Rare:41 | ||||
| chr5:132866435-132866713 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963286-132963363 | Rare:14 | ||||
| chr5:132963599-132963742 | Rare:43 | ||||
| chr5:133026504-133026754 | Common:4; Rare:66 | ||||
| chr5:133051843-133052355 | Common:1; Rare:165 | ||||
| chr5:133612486-133612743 | Common:1; Rare:61 | ||||
| chr5:133968547-133968726 | Rare:74 | ||||
| chr5:134004516-134005081 | Common:2; Rare:171 | ||||
| chr5:134176783-134177076 | Common:5; Rare:103 | ||||
| chr5:134225476-134225593 | Common:1; Rare:39 | ||||
| chr5:134225995-134226460 | Common:1; Rare:153 | ||||
| chr5:134367129-134367270 | Common:1; Rare:44 |