| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69369464-69369877 | Common:1; Rare:171 | ||||
| chr5:69370017-69370093 | Rare:11 | ||||
| chr5:72179360-72179789 | Common:1; Rare:90 | ||||
| chr5:72816524-72816718 | Common:4; Rare:72 | ||||
| chr5:72955741-72956080 | Common:1; Rare:137 | ||||
| chr5:73448775-73448889 | Rare:23 | ||||
| chr5:73498315-73498664 | Common:3; Rare:110 | ||||
| chr5:73498780-73499013 | Common:1; Rare:64 | ||||
| chr5:73565420-73565779 | Common:6; Rare:103 | ||||
| chr5:74767047-74767340 | Common:3; Rare:89 | ||||
| chr5:75336900-75337257 | Common:3; Rare:121 | ||||
| chr5:75511614-75511913 | Common:1; Rare:111 | ||||
| chr5:75717372-75717640 | Common:4; Rare:66 | ||||
| chr5:78360413-78360683 | Common:4; Rare:102 | ||||
| chr5:79069627-79069777 | Rare:52; Clinvar (benign):2 |