Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2213181-2213276 | Common:1; Rare:32 | ||||
chr1:2229171-2229249 | Common:1; Rare:22; Clinvar:2; Clinvar (benign):3 | ||||
chr1:2385047-2385202 | Common:2; Rare:61 | ||||
chr1:2391119-2391250 | Common:1; Rare:31 | ||||
chr1:2391424-2391873 | Common:2; Rare:171 | ||||
chr1:2412330-2412851 | Common:2; Rare:198; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:2526173-2526393 | Common:1; Rare:58 | ||||
chr1:2526499-2526753 | Common:4; Rare:98 | ||||
chr1:2556117-2556389 | Common:2; Rare:99 | ||||
chr1:2556533-2556676 | Rare:59 | ||||
chr1:2586308-2586523 | Common:1; Rare:70 | ||||
chr1:2586563-2586897 | Common:3; Rare:85 | ||||
chr1:3454357-3454493 | Rare:35 | ||||
chr1:3471484-3471633 | Common:2; Rare:36 | ||||
chr1:3471898-3471971 | Rare:14 |