Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:134845824-134846129 | Rare:134 | ||||
chr5:134846334-134846462 | Rare:38 | ||||
chr5:134873623-134873770 | Rare:32 | ||||
chr5:134874262-134874586 | Common:1; Rare:144 | ||||
chr5:135399069-135399325 | Rare:66 | ||||
chr5:136132763-136132971 | Common:1; Rare:62 | ||||
chr5:137735793-137735936 | Common:1; Rare:33; Clinvar (benign):2 | ||||
chr5:137754323-137754519 | Rare:68 | ||||
chr5:138032663-138032780 | Common:1; Rare:26 | ||||
chr5:138032949-138033208 | Common:1; Rare:89 | ||||
chr5:138178604-138178738 | Rare:32 | ||||
chr5:138337736-138337820 | Common:1; Rare:20 | ||||
chr5:138337955-138338296 | Common:2; Rare:131 | ||||
chr5:138464896-138465203 | Rare:79 | ||||
chr5:138465316-138465599 | Common:1; Rare:76 |