Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174999154-174999471 | Common:1; Rare:75 | ||||
chr1:174999644-175000145 | Common:3; Rare:156 | ||||
chr1:178094387-178094610 | Rare:91 | ||||
chr1:178341318-178341556 | Common:1; Rare:46 | ||||
chr1:179882119-179882360 | Common:1; Rare:45 | ||||
chr1:179882591-179882841 | Rare:120; Clinvar:6; Clinvar (benign):1 | ||||
chr1:179954481-179954809 | Common:3; Rare:80 | ||||
chr1:180631867-180632179 | Common:5; Rare:114 | ||||
chr1:182789656-182789778 | Common:2; Rare:39 | ||||
chr1:183472261-183472525 | Common:2; Rare:92 | ||||
chr1:183635655-183636109 | Common:5; Rare:128 | ||||
chr1:184051710-184051759 | Common:1; Rare:20 | ||||
chr1:184386627-184387154 | Common:3; Rare:147 | ||||
chr1:184974300-184974641 | Rare:99 | ||||
chr1:185156660-185156748 | Rare:47 |