| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126595183-126595345 | Common:3; Rare:75; Clinvar:4; Clinvar (benign):8 | ||||
| chr5:127030526-127030768 | Common:2; Rare:55 | ||||
| chr5:127517507-127517704 | Common:5; Rare:90 | ||||
| chr5:128538207-128538392 | Common:5; Rare:61 | ||||
| chr5:131170698-131171002 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr5:131635149-131635430 | Common:1; Rare:109 | ||||
| chr5:131796975-131797202 | Rare:63 | ||||
| chr5:132257475-132257749 | Common:8; Rare:73 | ||||
| chr5:132410601-132410613 | Rare:3 | ||||
| chr5:132490764-132491060 | Rare:77 | ||||
| chr5:132556836-132557003 | Common:1; Rare:60; Clinvar:1 | ||||
| chr5:132830617-132830781 | Rare:44 | ||||
| chr5:133026526-133026591 | Rare:25 | ||||
| chr5:133051851-133052268 | Rare:144 | ||||
| chr5:133968565-133968772 | Rare:85 |