| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131170670-131171038 | Common:1; Rare:91; Clinvar (benign):2 | ||||
| chr5:131245232-131245524 | Common:1; Rare:56 | ||||
| chr5:131263466-131263769 | Rare:77 | ||||
| chr5:131263900-131264133 | Common:1; Rare:86 | ||||
| chr5:131635090-131635404 | Common:1; Rare:109 | ||||
| chr5:131796922-131797227 | Rare:87 | ||||
| chr5:131945623-131945780 | Common:1; Rare:61 | ||||
| chr5:132011126-132011358 | Rare:47 | ||||
| chr5:132257507-132257703 | Common:6; Rare:40 | ||||
| chr5:132369589-132369964 | Common:8; Rare:124; Clinvar:6; Clinvar (benign):6 | ||||
| chr5:132370164-132370191 | Rare:11; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr5:132410746-132411017 | Rare:56 | ||||
| chr5:132490770-132490983 | Rare:46 | ||||
| chr5:132556772-132557226 | Common:1; Rare:150; Clinvar:1 | ||||
| chr5:132656107-132656565 | Common:2; Rare:118 |