Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:13348017-13348112 | Rare:20 | ||||
chr10:14838029-14838371 | Common:2; Rare:92 | ||||
chr10:14878634-14878894 | Common:2; Rare:77 | ||||
chr10:15860447-15860589 | Rare:39 | ||||
chr10:17201635-17201745 | Common:1; Rare:36 | ||||
chr10:17233557-17233930 | Common:3; Rare:117; Clinvar (benign):1 | ||||
chr10:17643850-17644317 | Common:2; Rare:150 | ||||
chr10:18659236-18659666 | Common:2; Rare:149 | ||||
chr10:18659767-18659831 | Rare:14 | ||||
chr10:25016413-25016681 | Common:8; Rare:100 | ||||
chr10:26860856-26861089 | Common:2; Rare:80 | ||||
chr10:27154176-27154486 | Rare:86 | ||||
chr10:27242079-27242211 | Common:1; Rare:56 | ||||
chr10:28532612-28532826 | Common:1; Rare:92 | ||||
chr10:28532975-28533140 | Rare:57 |