| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:122845516-122845687 | Common:3; Rare:66 | ||||
| chr5:123036359-123036494 | Rare:41 | ||||
| chr5:123036672-123037004 | Common:2; Rare:79 | ||||
| chr5:123423279-123423599 | Rare:106 | ||||
| chr5:124746596-124746844 | Common:1; Rare:52 | ||||
| chr5:124748777-124748987 | Common:2; Rare:48 | ||||
| chr5:126423321-126423510 | Rare:48 | ||||
| chr5:127030352-127030764 | Common:4; Rare:99 | ||||
| chr5:128083903-128084320 | Common:4; Rare:118 | ||||
| chr5:131165095-131165394 | Common:3; Rare:112; Clinvar (benign):2 | ||||
| chr5:131170716-131171032 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr5:131635184-131635257 | Rare:34 | ||||
| chr5:131796967-131797202 | Rare:66 | ||||
| chr5:132369897-132369915 | Rare:4 | ||||
| chr5:132387650-132387845 | Common:1; Rare:34 |