Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39026731-39026844 | Common:1; Rare:27 | ||||
chr1:39105235-39105435 | Common:2; Rare:56 | ||||
chr1:39408569-39408690 | Rare:32 | ||||
chr1:39408718-39409099 | Common:5; Rare:141 | ||||
chr1:39491523-39491722 | Common:4; Rare:64 | ||||
chr1:39576785-39576982 | Rare:67 | ||||
chr1:39639611-39639875 | Rare:97 | ||||
chr1:39639934-39640101 | Common:1; Rare:36 | ||||
chr1:39691394-39691601 | Common:5; Rare:43 | ||||
chr1:39738701-39739022 | Common:3; Rare:84 | ||||
chr1:39788757-39789163 | Common:4; Rare:124 | ||||
chr1:39883440-39883632 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:39901666-39902116 | Common:6; Rare:135 | ||||
chr1:39954965-39955159 | Common:1; Rare:51 | ||||
chr1:40039744-40040097 | Common:2; Rare:86 |