| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127030507-127030764 | Common:2; Rare:61 | ||||
| chr5:131170678-131170988 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr5:131635160-131635466 | Common:1; Rare:117 | ||||
| chr5:131796948-131797221 | Rare:76 | ||||
| chr5:132410603-132410945 | Common:1; Rare:67 | ||||
| chr5:132490761-132491060 | Rare:78 | ||||
| chr5:132556836-132557020 | Common:1; Rare:66; Clinvar:1 | ||||
| chr5:132866435-132866681 | Common:1; Rare:78; Clinvar (benign):1 | ||||
| chr5:132963293-132963825 | Common:4; Rare:131 | ||||
| chr5:133026533-133026727 | Common:3; Rare:47 | ||||
| chr5:133051862-133052306 | Common:1; Rare:144 | ||||
| chr5:133968571-133968688 | Rare:55 | ||||
| chr5:134004521-134004855 | Common:1; Rare:113 | ||||
| chr5:134004910-134005104 | Rare:41 | ||||
| chr5:134226025-134226407 | Common:1; Rare:124 |