Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23080705-23080758 | Common:1; Rare:10 | ||||
chr1:23344214-23344378 | Common:2; Rare:75 | ||||
chr1:23368288-23368486 | Common:1; Rare:53 | ||||
chr1:23368858-23369255 | Common:3; Rare:107 | ||||
chr1:23558896-23559150 | Common:5; Rare:124 | ||||
chr1:23559471-23559643 | Common:1; Rare:74 | ||||
chr1:23581226-23581525 | Rare:74 | ||||
chr1:23778285-23778451 | Common:6; Rare:87 | ||||
chr1:23791870-23791986 | Rare:21 | ||||
chr1:23793029-23793217 | Common:1; Rare:61 | ||||
chr1:23825358-23825539 | Common:3; Rare:62; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr1:23961239-23961465 | Common:5; Rare:45 | ||||
chr1:23975194-23975398 | Common:1; Rare:45 | ||||
chr1:23975527-23975690 | Common:1; Rare:25 | ||||
chr1:23980203-23980498 | Rare:80 |