Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149812203-149812619 | Common:8; Rare:413 | ||||
chr1:149886407-149887317 | Common:9; Rare:787 | ||||
chr1:149887302-149888300 | Rare:840 | ||||
chr1:149899260-149899691 | Common:3; Rare:111 | ||||
chr1:149899776-149899937 | Rare:33 | ||||
chr1:149926511-149927558 | Common:5; Rare:354; Clinvar (benign):2 | ||||
chr1:149927705-149928045 | Common:4; Rare:306; Clinvar:2; Clinvar (benign):16 | ||||
chr1:149928114-149928256 | Common:1; Rare:26 | ||||
chr1:149936701-149937101 | Common:3; Rare:122 | ||||
chr1:149937363-149937656 | Common:2; Rare:47 | ||||
chr1:150010579-150010970 | Common:5; Rare:183 | ||||
chr1:150067079-150067480 | Common:11; Rare:182 | ||||
chr1:150067417-150067933 | Common:3; Rare:289 | ||||
chr1:150149690-150150247 | Common:7; Rare:389 | ||||
chr1:150234593-150235000 | Rare:130 |