| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127030509-127030768 | Common:2; Rare:62 | ||||
| chr5:127290657-127290846 | Rare:41 | ||||
| chr5:128083596-128083766 | Common:2; Rare:70 | ||||
| chr5:128083926-128084710 | Common:6; Rare:251 | ||||
| chr5:128965423-128965594 | Common:2; Rare:49 | ||||
| chr5:129094467-129094937 | Common:3; Rare:205 | ||||
| chr5:131170707-131171008 | Common:1; Rare:61; Clinvar (benign):2 | ||||
| chr5:131263911-131264117 | Rare:76 | ||||
| chr5:131635141-131635398 | Common:1; Rare:100 | ||||
| chr5:131796936-131797221 | Rare:81 | ||||
| chr5:132257475-132257815 | Common:8; Rare:86 | ||||
| chr5:132369602-132369759 | Common:3; Rare:46 | ||||
| chr5:132369883-132369936 | Common:2; Rare:17; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:132370138-132370219 | Rare:31; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:132410603-132410995 | Common:1; Rare:81 |