| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140664791-140664930 | Common:2; Rare:41 | ||||
| chr5:140691300-140691675 | Common:1; Rare:137; Clinvar:12; Clinvar (benign):2 | ||||
| chr5:141172537-141172667 | Common:1; Rare:26 | ||||
| chr5:141320742-141320920 | Common:1; Rare:62 | ||||
| chr5:141636810-141637011 | Common:2; Rare:86 | ||||
| chr5:141637374-141637478 | Rare:22 | ||||
| chr5:141869558-141869749 | Rare:45 | ||||
| chr5:141923736-141923904 | Common:1; Rare:46 | ||||
| chr5:142013001-142013088 | Rare:26 | ||||
| chr5:142324992-142325188 | Rare:68 | ||||
| chr5:143404442-143404617 | Common:2; Rare:36 | ||||
| chr5:145937633-145937821 | Rare:50 | ||||
| chr5:146182497-146182848 | Common:3; Rare:95 | ||||
| chr5:147509895-147510277 | Common:1; Rare:76 | ||||
| chr5:148090361-148090430 | Rare:8 |