| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131635160-131635446 | Common:1; Rare:109 | ||||
| chr5:131796928-131797246 | Rare:93 | ||||
| chr5:132011597-132011763 | Rare:50 | ||||
| chr5:132257488-132257715 | Common:7; Rare:55 | ||||
| chr5:132369628-132369752 | Common:2; Rare:35 | ||||
| chr5:132369882-132369964 | Common:2; Rare:31; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:132490774-132491020 | Rare:64 | ||||
| chr5:132556821-132556997 | Common:1; Rare:60; Clinvar:1 | ||||
| chr5:132737416-132737732 | Rare:110 | ||||
| chr5:132777150-132777442 | Common:3; Rare:73 | ||||
| chr5:132866333-132866722 | Common:3; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133026504-133026624 | Common:1; Rare:46 | ||||
| chr5:133051862-133052355 | Common:1; Rare:156 | ||||
| chr5:133968541-133968722 | Rare:75 | ||||
| chr5:134004516-134004911 | Common:2; Rare:135 |