| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:141929408-141929710 | Common:2; Rare:84 | ||||
| chr5:141935958-141936015 | Rare:12 | ||||
| chr5:142151459-142152102 | Common:1; Rare:94 | ||||
| chr5:143082040-143082081 | Rare:6 | ||||
| chr5:143132879-143133070 | Rare:32 | ||||
| chr5:143275647-143275838 | Common:1; Rare:27 | ||||
| chr5:143282699-143282753 | Common:1; Rare:9; Clinvar (benign):1 | ||||
| chr5:143291109-143291145 | Rare:8 | ||||
| chr5:143311808-143312074 | Common:3; Rare:38 | ||||
| chr5:143391779-143391808 | Rare:6 | ||||
| chr5:146058473-146058861 | Common:2; Rare:60 | ||||
| chr5:146063886-146064616 | Common:15; Rare:131 | ||||
| chr5:146065573-146065736 | Common:3; Rare:23 | ||||
| chr5:146075802-146075862 | Rare:13 | ||||
| chr5:146105438-146105571 | Rare:10 |