Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11012259-11012447 | Rare:48 | ||||
chr1:11012613-11012742 | Common:1; Rare:44; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11012874-11012964 | Rare:35 | ||||
chr1:11013063-11013119 | Rare:21 | ||||
chr1:11013506-11013757 | Rare:62; Clinvar (benign):1 | ||||
chr1:11059894-11060343 | Common:3; Rare:150 | ||||
chr1:11072101-11072357 | Common:1; Rare:51 | ||||
chr1:11099740-11099933 | Common:3; Rare:80 | ||||
chr1:11189261-11189355 | Rare:17 | ||||
chr1:11262434-11262836 | Common:2; Rare:115 | ||||
chr1:11272922-11273234 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11273430-11273514 | Common:1; Rare:29; Clinvar (benign):1 | ||||
chr1:11478847-11479157 | Common:3; Rare:90 | ||||
chr1:11654339-11654505 | Rare:49 | ||||
chr1:11654806-11655064 | Common:3; Rare:60 |