Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:31644852-31645002 | Common:3; Rare:48 | ||||
chr1:32292035-32292215 | Rare:67 | ||||
chr1:32650929-32651226 | Common:2; Rare:99 | ||||
chr1:32817294-32817679 | Rare:96; Clinvar:5 | ||||
chr1:34985303-34985389 | Common:1; Rare:27 | ||||
chr1:35181742-35181875 | Rare:29 | ||||
chr1:35193108-35193159 | Rare:28 | ||||
chr1:35557373-35557465 | Rare:18 | ||||
chr1:35557597-35557834 | Common:2; Rare:86 | ||||
chr1:35641459-35641629 | Rare:37 | ||||
chr1:36149420-36149822 | Common:3; Rare:111 | ||||
chr1:36155847-36156163 | Rare:118 | ||||
chr1:36464236-36464490 | Common:2; Rare:75 | ||||
chr1:36467556-36467851 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
chr1:36472242-36472678 | Common:4; Rare:140; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 |