Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:13099949-13100205 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):4 | ||||
chr10:14837987-14838345 | Common:2; Rare:100 | ||||
chr10:14878651-14878881 | Common:2; Rare:65 | ||||
chr10:15097301-15097378 | Common:1; Rare:37 | ||||
chr10:17228404-17228675 | Common:3; Rare:70 | ||||
chr10:17643871-17644265 | Common:2; Rare:119 | ||||
chr10:18651577-18651720 | Common:1; Rare:57 | ||||
chr10:18659292-18659606 | Common:1; Rare:102 | ||||
chr10:19816270-19816496 | Common:5; Rare:40 | ||||
chr10:21534017-21534245 | Common:1; Rare:72 | ||||
chr10:24208858-24209184 | Rare:93 | ||||
chr10:27154310-27154514 | Rare:59 | ||||
chr10:27155264-27155390 | Common:3; Rare:44; Clinvar:1; Clinvar (benign):3 | ||||
chr10:27240481-27240805 | Common:2; Rare:100 | ||||
chr10:27242086-27242217 | Common:1; Rare:51 |