Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23559130-23559171 | Rare:19 | ||||
chr1:23559173-23559259 | Rare:34 | ||||
chr1:23559411-23559648 | Common:1; Rare:102 | ||||
chr1:23691540-23691829 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
chr1:23778281-23778492 | Common:9; Rare:110 | ||||
chr1:23791075-23791241 | Rare:49 | ||||
chr1:23799534-23799702 | Rare:24 | ||||
chr1:23800732-23800959 | Common:1; Rare:80 | ||||
chr1:23959069-23959328 | Common:3; Rare:49 | ||||
chr1:23959641-23959920 | Common:2; Rare:73 | ||||
chr1:23980243-23980484 | Rare:74 | ||||
chr1:24187206-24187513 | Common:9; Rare:88 | ||||
chr1:24642882-24643348 | Common:2; Rare:153 | ||||
chr1:24745295-24745608 | Common:2; Rare:110 | ||||
chr1:24929255-24929390 | Common:1; Rare:57 |