| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131263918-131264109 | Rare:70 | ||||
| chr5:131635183-131635422 | Common:1; Rare:91 | ||||
| chr5:131796948-131797215 | Rare:75 | ||||
| chr5:132369589-132369936 | Common:8; Rare:110; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:132410603-132410956 | Common:1; Rare:68 | ||||
| chr5:132490774-132490989 | Rare:51 | ||||
| chr5:132866471-132866694 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963281-132963403 | Rare:25 | ||||
| chr5:133051862-133052355 | Common:1; Rare:156 | ||||
| chr5:133968573-133968688 | Rare:54 | ||||
| chr5:134004647-134004855 | Common:1; Rare:77 | ||||
| chr5:134226009-134226402 | Common:1; Rare:128 | ||||
| chr5:134371026-134371184 | Common:1; Rare:41 | ||||
| chr5:134385006-134385176 | Rare:37 | ||||
| chr5:134411846-134411981 | Rare:46 |