| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:84384378-84384514 | Rare:39 | ||||
| chr5:84384610-84384714 | Rare:54 | ||||
| chr5:87267722-87267995 | Common:4; Rare:92 | ||||
| chr5:87268671-87268978 | Common:1; Rare:136; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:87401699-87401915 | Rare:57 | ||||
| chr5:87412290-87412406 | Rare:22 | ||||
| chr5:87412600-87412627 | Rare:6 | ||||
| chr5:87412740-87413127 | Common:4; Rare:126 | ||||
| chr5:88827131-88827463 | Rare:49 | ||||
| chr5:88882987-88883399 | Rare:99; Clinvar:7; Clinvar (benign):3 | ||||
| chr5:90409711-90410024 | Common:6; Rare:102 | ||||
| chr5:90474352-90474502 | Rare:59 | ||||
| chr5:90474660-90474915 | Common:2; Rare:93 | ||||
| chr5:90529506-90529819 | Common:1; Rare:122 | ||||
| chr5:91380063-91380378 | Common:2; Rare:89 |