Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:43065690-43066017 | Common:3; Rare:54 | ||||
chr5:43066345-43066455 | Common:3; Rare:33 | ||||
chr5:43066921-43067066 | Rare:51 | ||||
chr5:51378497-51378727 | Common:1; Rare:38 | ||||
chr5:55944379-55944618 | Rare:51 | ||||
chr5:65925581-65925932 | Rare:135 | ||||
chr5:68251917-68252183 | Common:1; Rare:38 | ||||
chr5:75052510-75052649 | Common:2; Rare:34 | ||||
chr5:77080568-77080798 | Common:1; Rare:52 | ||||
chr5:80650902-80651186 | Common:2; Rare:55 | ||||
chr5:87369544-87369847 | Rare:44; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr5:93585576-93585711 | Rare:27 | ||||
chr5:93621453-93621690 | Common:3; Rare:65 | ||||
chr5:96934232-96934471 | Common:1; Rare:45 | ||||
chr5:109355966-109356127 | Common:4; Rare:43 |