Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:75724542-75724815 | Common:2; Rare:118; Clinvar:5; Clinvar (benign):2 | ||||
chr1:75785934-75786310 | Common:4; Rare:136 | ||||
chr1:75786698-75786742 | Rare:17 | ||||
chr1:76074516-76074772 | Common:2; Rare:100 | ||||
chr1:77219251-77219557 | Common:1; Rare:137 | ||||
chr1:77682557-77682734 | Rare:42 | ||||
chr1:77682914-77683291 | Common:3; Rare:79 | ||||
chr1:77683311-77683714 | Common:1; Rare:120 | ||||
chr1:77683852-77683941 | Rare:20 | ||||
chr1:77759560-77759572 | Rare:1 | ||||
chr1:77759670-77759946 | Common:2; Rare:111 | ||||
chr1:77779531-77779873 | Rare:106 | ||||
chr1:77888073-77888219 | Rare:44 | ||||
chr1:77888535-77888853 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77978780-77978870 | Rare:24 |