| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140700270-140700490 | Rare:76 | ||||
| chr5:140806835-140807090 | Common:3; Rare:46 | ||||
| chr5:141320715-141320928 | Common:3; Rare:75 | ||||
| chr5:141343792-141343893 | Rare:24 | ||||
| chr5:141475837-141476016 | Rare:37 | ||||
| chr5:141484856-141485069 | Common:1; Rare:40 | ||||
| chr5:141560786-141561077 | Common:4; Rare:75 | ||||
| chr5:141618910-141619243 | Common:1; Rare:106; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:141636803-141637011 | Common:2; Rare:93 | ||||
| chr5:141637329-141637478 | Common:1; Rare:35 | ||||
| chr5:141923721-141923904 | Common:1; Rare:52 | ||||
| chr5:141924077-141924105 | Rare:6 | ||||
| chr5:141968962-141969275 | Common:3; Rare:97 | ||||
| chr5:142012990-142013157 | Common:2; Rare:49 | ||||
| chr5:142108675-142108966 | Common:3; Rare:99 |