Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:24209015-24209184 | Rare:50 | ||||
chr10:24722704-24722878 | Common:1; Rare:45 | ||||
chr10:27100427-27100587 | Common:3; Rare:49; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154310-27154480 | Rare:45 | ||||
chr10:27155197-27155416 | Common:7; Rare:95; Clinvar:3; Clinvar (benign):7 | ||||
chr10:27240474-27240886 | Common:2; Rare:121 | ||||
chr10:27242058-27242245 | Common:1; Rare:82 | ||||
chr10:27745472-27745671 | Rare:44 | ||||
chr10:27746210-27746224 | |||||
chr10:28532719-28532880 | Common:1; Rare:56 | ||||
chr10:28533032-28533199 | Rare:66 | ||||
chr10:29634899-29635071 | Rare:35 | ||||
chr10:29735768-29735983 | Common:3; Rare:40 | ||||
chr10:29736635-29736724 | Rare:20 | ||||
chr10:29736741-29737083 | Common:2; Rare:95 |