| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140303065-140303160 | Common:1; Rare:28 | ||||
| chr5:140557419-140557771 | Common:3; Rare:133 | ||||
| chr5:140564619-140564853 | Rare:64 | ||||
| chr5:140647594-140647880 | Common:5; Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691305-140691485 | Common:1; Rare:66; Clinvar:7 | ||||
| chr5:141636809-141636997 | Common:2; Rare:82 | ||||
| chr5:142324979-142325236 | Rare:86 | ||||
| chr5:143404457-143404604 | Common:2; Rare:30 | ||||
| chr5:148383786-148383973 | Rare:50 | ||||
| chr5:149063050-149063380 | Rare:66; Clinvar:1 | ||||
| chr5:149551366-149551744 | Common:1; Rare:97 | ||||
| chr5:149960575-149960923 | Rare:116; Clinvar:7 | ||||
| chr5:150412857-150413129 | Common:1; Rare:40 | ||||
| chr5:150449639-150449795 | Common:4; Rare:50 | ||||
| chr5:150700981-150701147 | Common:2; Rare:72 |