Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22316228-22316478 | Common:2; Rare:117 | ||||
chr10:22325539-22325661 | Rare:54 | ||||
chr10:27100461-27100594 | Common:3; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
chr10:27154310-27154470 | Rare:44 | ||||
chr10:27155252-27155419 | Common:6; Rare:76; Clinvar:2; Clinvar (benign):6 | ||||
chr10:27242058-27242241 | Common:1; Rare:78 | ||||
chr10:28532423-28532847 | Common:5; Rare:156 | ||||
chr10:29634879-29635071 | Rare:40 | ||||
chr10:30059503-30059666 | Common:1; Rare:61 | ||||
chr10:31031841-31032050 | Common:2; Rare:84 | ||||
chr10:31319063-31319251 | Common:2; Rare:57 | ||||
chr10:31928792-31928913 | Common:2; Rare:46 | ||||
chr10:32378684-32378900 | Common:1; Rare:27 | ||||
chr10:32446059-32446297 | Common:1; Rare:105 | ||||
chr10:32958160-32958472 | Common:2; Rare:121 |