| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140557427-140557548 | Common:2; Rare:73 | ||||
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140647557-140647883 | Common:5; Rare:135; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691305-140691641 | Common:1; Rare:119; Clinvar:9; Clinvar (benign):1 | ||||
| chr5:141320747-141320928 | Common:2; Rare:60 | ||||
| chr5:141636794-141637011 | Common:2; Rare:101 | ||||
| chr5:141682195-141682328 | Common:1; Rare:43 | ||||
| chr5:141923741-141923881 | Common:1; Rare:31 | ||||
| chr5:142325017-142325183 | Rare:55 | ||||
| chr5:143404455-143404604 | Common:2; Rare:31 | ||||
| chr5:145835280-145835499 | Common:2; Rare:52 | ||||
| chr5:145937638-145937761 | Rare:31 | ||||
| chr5:146182501-146182886 | Common:4; Rare:115 | ||||
| chr5:148383838-148384039 | Rare:60 | ||||
| chr5:149141420-149141742 | Rare:88 |