| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131635172-131635398 | Common:1; Rare:86 | ||||
| chr5:131796948-131797208 | Rare:74 | ||||
| chr5:132294138-132294424 | Common:1; Rare:69 | ||||
| chr5:132295333-132295453 | Rare:24 | ||||
| chr5:132369323-132369561 | Common:3; Rare:57 | ||||
| chr5:132369897-132369988 | Rare:35; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr5:132556770-132557045 | Common:1; Rare:90; Clinvar:1 | ||||
| chr5:132557215-132557453 | Common:1; Rare:65; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr5:132737424-132737652 | Rare:85 | ||||
| chr5:132866467-132866676 | Common:1; Rare:65 | ||||
| chr5:132963489-132963746 | Rare:70 | ||||
| chr5:133051861-133052209 | Rare:114 | ||||
| chr5:133968582-133968747 | Rare:62 | ||||
| chr5:134004497-134004921 | Common:2; Rare:143 | ||||
| chr5:134004973-134005125 | Rare:34 |