Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62436253-62436318 | Common:1; Rare:18 | ||||
chr1:62437015-62437055 | Common:1; Rare:13 | ||||
chr1:62688256-62688510 | Common:1; Rare:101; Clinvar:1 | ||||
chr1:62784073-62784180 | Rare:44 | ||||
chr1:63367508-63367671 | Rare:45 | ||||
chr1:63523161-63523592 | Common:3; Rare:117 | ||||
chr1:63593659-63593699 | Rare:19; Clinvar (pathogenic):1 | ||||
chr1:63593723-63593881 | Common:2; Rare:74 | ||||
chr1:66332191-66332479 | Rare:77 | ||||
chr1:66533443-66533659 | Common:2; Rare:33 | ||||
chr1:66534017-66534169 | Common:1; Rare:33 | ||||
chr1:66924845-66925024 | Rare:77 | ||||
chr1:66925196-66925518 | Common:2; Rare:100 | ||||
chr1:67833342-67833568 | Common:3; Rare:87 | ||||
chr1:68232421-68232661 | Common:1; Rare:53 |