| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915472-34915741 | Common:1; Rare:65 | ||||
| chr5:36151885-36152174 | Rare:91 | ||||
| chr5:36876650-36876907 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:39074363-39074530 | Common:1; Rare:76 | ||||
| chr5:40679753-40679929 | Rare:34 | ||||
| chr5:40755902-40756018 | Rare:33 | ||||
| chr5:40798158-40798401 | Common:1; Rare:89 | ||||
| chr5:43121365-43121648 | Common:1; Rare:108 | ||||
| chr5:43313408-43313665 | Common:3; Rare:67 | ||||
| chr5:43483837-43483896 | Common:1; Rare:28 | ||||
| chr5:43515128-43515275 | Common:3; Rare:56 | ||||
| chr5:43602867-43603280 | Rare:100 | ||||
| chr5:44808727-44808976 | Common:2; Rare:84 | ||||
| chr5:53109725-53109904 | Common:1; Rare:90; Clinvar:2 | ||||
| chr5:54310507-54310711 | Rare:65 |