| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132227761-132227950 | Common:2; Rare:45 | ||||
| chr5:132369635-132369740 | Common:2; Rare:29 | ||||
| chr5:132556832-132557045 | Common:1; Rare:77; Clinvar:1 | ||||
| chr5:132557410-132557453 | Rare:14; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:132777212-132777351 | Rare:31 | ||||
| chr5:132866467-132866692 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963509-132963803 | Common:1; Rare:74 | ||||
| chr5:133026504-133026755 | Common:4; Rare:66 | ||||
| chr5:133051862-133052103 | Rare:90 | ||||
| chr5:133101596-133101877 | Common:3; Rare:55 | ||||
| chr5:133968552-133968707 | Rare:68 | ||||
| chr5:133980667-133980775 | Common:3; Rare:26 | ||||
| chr5:134004659-134004919 | Common:1; Rare:96 | ||||
| chr5:134114538-134114779 | Rare:75 | ||||
| chr5:134176873-134177069 | Common:4; Rare:86 |