| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132260172-132261074 | Common:7; Rare:198 | ||||
| chr5:132278397-132278760 | Common:3; Rare:101 | ||||
| chr5:132293800-132294734 | Common:11; Rare:902 | ||||
| chr5:132295181-132295584 | Common:4; Rare:246 | ||||
| chr5:132295563-132296141 | Common:4; Rare:176 | ||||
| chr5:132369080-132370392 | Common:87; Rare:1901; Clinvar:110; Clinvar (benign):71; Clinvar (pathogenic):90 | ||||
| chr5:132370742-132371515 | Common:7; Rare:144 | ||||
| chr5:132409969-132410650 | Rare:159 | ||||
| chr5:132410603-132411240 | Common:13; Rare:565 | ||||
| chr5:132419551-132420008 | Common:5; Rare:209 | ||||
| chr5:132420151-132420551 | Common:4; Rare:97 | ||||
| chr5:132489987-132490387 | Common:1; Rare:83 | ||||
| chr5:132490720-132491100 | Common:2; Rare:376 | ||||
| chr5:132556410-132557313 | Common:8; Rare:905; Clinvar:7; Clinvar (benign):2 | ||||
| chr5:132557310-132557480 | Rare:48; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):3 |