Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:78360406-78360666 | Common:5; Rare:99 | ||||
chr5:79991208-79991337 | Rare:39 | ||||
chr5:80256013-80256209 | Common:1; Rare:80 | ||||
chr5:81301513-81301698 | Common:4; Rare:66 | ||||
chr5:82278319-82278660 | Common:3; Rare:108 | ||||
chr5:83077330-83077605 | Common:1; Rare:84 | ||||
chr5:87268655-87268967 | Common:1; Rare:138; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr5:87412836-87412961 | Common:2; Rare:42 | ||||
chr5:90409730-90410033 | Common:7; Rare:99 | ||||
chr5:90529521-90529811 | Common:1; Rare:109 | ||||
chr5:91380054-91380388 | Common:3; Rare:94 | ||||
chr5:91383273-91383426 | Rare:45 | ||||
chr5:94111522-94111747 | Common:2; Rare:84 | ||||
chr5:95554951-95555183 | Rare:63 | ||||
chr5:95731512-95731801 | Rare:110 |