Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:24466372-24466554 | Rare:31 | ||||
chr10:27100473-27100582 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
chr10:27154315-27154480 | Rare:43 | ||||
chr10:27155165-27155419 | Common:7; Rare:107; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240565-27240866 | Common:2; Rare:79 | ||||
chr10:27242079-27242212 | Common:1; Rare:56 | ||||
chr10:28532463-28532862 | Common:5; Rare:156 | ||||
chr10:28533036-28533188 | Rare:59 | ||||
chr10:29634930-29634958 | Rare:11 | ||||
chr10:29735781-29736035 | Common:3; Rare:52 | ||||
chr10:30349277-30349377 | Common:11; Rare:72 | ||||
chr10:31031839-31032044 | Common:2; Rare:81 | ||||
chr10:31319042-31319228 | Common:2; Rare:57 | ||||
chr10:31928767-31928927 | Common:2; Rare:64 | ||||
chr10:32446068-32446149 | Common:1; Rare:37 |