Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147172163-147172804 | Common:1; Rare:168 | ||||
chr1:147541283-147541569 | Common:1; Rare:46 | ||||
chr1:147670512-147670822 | Common:2; Rare:70 | ||||
chr1:147928321-147928398 | Rare:24 | ||||
chr1:149886679-149886951 | Rare:81 | ||||
chr1:149927757-149927910 | Common:1; Rare:62; Clinvar (benign):5 | ||||
chr1:150067593-150067876 | Common:1; Rare:78 | ||||
chr1:150149856-150150206 | Common:2; Rare:123 | ||||
chr1:150235731-150235931 | Common:2; Rare:35 | ||||
chr1:150235942-150236045 | Rare:20 | ||||
chr1:150272371-150272781 | Common:1; Rare:74 | ||||
chr1:150282285-150282598 | Common:3; Rare:65 | ||||
chr1:150321359-150321595 | Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150629549-150629836 | Rare:59 | ||||
chr1:151008391-151008480 | Common:1; Rare:33 |