Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32179563-32179758 | Rare:43 | ||||
chr1:32200532-32200685 | Rare:34 | ||||
chr1:32205605-32205704 | Common:1; Rare:46 | ||||
chr1:32222294-32222444 | Rare:76 | ||||
chr1:32291824-32292156 | Common:1; Rare:95 | ||||
chr1:32464764-32465077 | Rare:72 | ||||
chr1:32650900-32651322 | Common:2; Rare:152 | ||||
chr1:32651715-32651968 | Rare:64 | ||||
chr1:32817302-32817674 | Rare:94; Clinvar:5 | ||||
chr1:33036826-33037082 | Rare:95; Clinvar (pathogenic):1 | ||||
chr1:35557353-35557486 | Common:1; Rare:36 | ||||
chr1:35557594-35557883 | Common:2; Rare:113 | ||||
chr1:36084037-36084114 | Common:2; Rare:25 | ||||
chr1:36088723-36088921 | Common:1; Rare:70 | ||||
chr1:36149439-36149753 | Common:2; Rare:84 |