Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:92355469-92355768 | Rare:49 | ||||
chr10:92481160-92481220 | Rare:5 | ||||
chr10:92554237-92554537 | Rare:44 | ||||
chr10:92572850-92572873 | Rare:6 | ||||
chr10:92573134-92573253 | Rare:26 | ||||
chr10:92591637-92591753 | Rare:39 | ||||
chr10:92608154-92608211 | Common:1; Rare:3 | ||||
chr10:92612780-92613118 | Common:3; Rare:54; Clinvar (pathogenic):1 | ||||
chr10:92628618-92628893 | Common:1; Rare:62 | ||||
chr10:92649600-92649850 | Common:1; Rare:53; Clinvar (benign):1 | ||||
chr10:92660393-92660422 | Common:1; Rare:8 | ||||
chr10:92669496-92669678 | Rare:26 | ||||
chr10:92690931-92691245 | Common:1; Rare:62 | ||||
chr10:92699693-92699961 | Common:2; Rare:51 | ||||
chr10:92830776-92830987 | Rare:24 |