Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:79991196-79991354 | Rare:50 | ||||
chr5:80256011-80256257 | Common:1; Rare:103 | ||||
chr5:80407856-80408102 | Common:1; Rare:92 | ||||
chr5:80487895-80488126 | Common:1; Rare:75 | ||||
chr5:80654392-80654706 | Common:5; Rare:152 | ||||
chr5:81301470-81301675 | Common:5; Rare:70 | ||||
chr5:81751034-81751400 | Common:1; Rare:101 | ||||
chr5:81971807-81972050 | Common:2; Rare:90 | ||||
chr5:82277692-82278027 | Common:1; Rare:85 | ||||
chr5:82278319-82278674 | Common:3; Rare:114 | ||||
chr5:83077330-83077615 | Common:1; Rare:85 | ||||
chr5:84384378-84384473 | Rare:25 | ||||
chr5:84384575-84384714 | Rare:66 | ||||
chr5:87267649-87267995 | Common:4; Rare:131 | ||||
chr5:87268135-87268269 | Common:2; Rare:33; Clinvar (benign):1 |