| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140346598-140346721 | Common:1; Rare:33 | ||||
| chr5:140557405-140557552 | Common:2; Rare:95 | ||||
| chr5:140564309-140564462 | Common:1; Rare:45 | ||||
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140647585-140647923 | Common:5; Rare:138; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664693-140664920 | Common:4; Rare:62 | ||||
| chr5:140691318-140691620 | Common:1; Rare:106; Clinvar:8; Clinvar (benign):1 | ||||
| chr5:141320737-141320920 | Common:2; Rare:63 | ||||
| chr5:141636809-141637011 | Common:2; Rare:86 | ||||
| chr5:141923730-141923904 | Common:1; Rare:48 | ||||
| chr5:142012960-142013069 | Rare:34 | ||||
| chr5:142108680-142108998 | Common:3; Rare:105 | ||||
| chr5:142325008-142325219 | Rare:66 | ||||
| chr5:142770171-142770377 | Rare:67 | ||||
| chr5:143404442-143404604 | Common:2; Rare:34 |