| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140257716-140257866 | Rare:25 | ||||
| chr5:140334085-140334416 | Common:2; Rare:43 | ||||
| chr5:140527792-140527903 | Common:1; Rare:27 | ||||
| chr5:140548767-140549031 | Common:1; Rare:80 | ||||
| chr5:140651536-140651805 | Common:2; Rare:63 | ||||
| chr5:140711181-140711275 | Common:1; Rare:24 | ||||
| chr5:141505244-141505474 | Common:1; Rare:50 | ||||
| chr5:141588247-141588305 | Rare:16; Clinvar (benign):1 | ||||
| chr5:141617969-141618200 | Rare:38 | ||||
| chr5:141849684-141849818 | Rare:34 | ||||
| chr5:142798463-142798493 | Rare:2 | ||||
| chr5:143044543-143044772 | Common:2; Rare:41 | ||||
| chr5:146126435-146126751 | Common:2; Rare:80; Clinvar (benign):3 | ||||
| chr5:147828997-147829272 | Common:8; Rare:43 | ||||
| chr5:148826431-148826650 | Common:2; Rare:62 |