| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:75717390-75717690 | Common:6; Rare:80 | ||||
| chr5:76818871-76819008 | Rare:44 | ||||
| chr5:77087201-77087490 | Rare:45 | ||||
| chr5:78360355-78360721 | Common:5; Rare:141 | ||||
| chr5:79069627-79069783 | Rare:54; Clinvar (benign):2 | ||||
| chr5:79612213-79612615 | Rare:107 | ||||
| chr5:79689705-79690064 | Common:3; Rare:106 | ||||
| chr5:79991176-79991337 | Rare:51 | ||||
| chr5:80256020-80256217 | Common:1; Rare:78 | ||||
| chr5:80407878-80408149 | Common:1; Rare:94 | ||||
| chr5:80487910-80488126 | Common:1; Rare:69 | ||||
| chr5:80654570-80654714 | Common:4; Rare:89 | ||||
| chr5:81233117-81233377 | Common:2; Rare:65 | ||||
| chr5:81301513-81301670 | Common:4; Rare:55 | ||||
| chr5:81751028-81751448 | Common:1; Rare:121 |