Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:75511607-75511917 | Common:1; Rare:112 | ||||
chr5:76623320-76623371 | Common:1; Rare:15 | ||||
chr5:77087196-77087456 | Rare:42 | ||||
chr5:78360365-78360667 | Common:5; Rare:116 | ||||
chr5:79069618-79069769 | Rare:53; Clinvar (benign):2 | ||||
chr5:79235951-79236135 | Common:2; Rare:74 | ||||
chr5:79991222-79991339 | Rare:36 | ||||
chr5:80256035-80256222 | Common:1; Rare:74 | ||||
chr5:80487901-80488129 | Common:1; Rare:73 | ||||
chr5:80654601-80654703 | Common:3; Rare:63 | ||||
chr5:81301479-81301693 | Common:5; Rare:74 | ||||
chr5:81971786-81972044 | Common:3; Rare:99 | ||||
chr5:82278319-82278705 | Common:4; Rare:127 | ||||
chr5:83077330-83077637 | Common:1; Rare:92 | ||||
chr5:84384351-84384506 | Rare:48 |