Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21783078-21783293 | Common:2; Rare:78 | ||||
chr1:22451706-22451879 | Common:1; Rare:59 | ||||
chr1:22636533-22636750 | Common:1; Rare:46 | ||||
chr1:22637409-22637778 | Common:3; Rare:85; Clinvar (benign):1 | ||||
chr1:22652935-22653303 | Common:1; Rare:76 | ||||
chr1:23019256-23019473 | Rare:52 | ||||
chr1:23344219-23344576 | Common:2; Rare:122 | ||||
chr1:23368133-23368513 | Common:2; Rare:112 | ||||
chr1:23368779-23369002 | Common:2; Rare:72 | ||||
chr1:23559015-23559037 | Rare:12 | ||||
chr1:23559386-23559661 | Common:2; Rare:119 | ||||
chr1:23778250-23778568 | Common:10; Rare:143 | ||||
chr1:23791047-23791231 | Rare:55 | ||||
chr1:23800739-23800959 | Common:1; Rare:76 | ||||
chr1:23825400-23825539 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |