Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100987268-100987599 | Common:1; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031132-101031275 | Rare:34 | ||||
chr10:101588211-101588333 | Rare:49 | ||||
chr10:101818350-101818752 | Common:1; Rare:110 | ||||
chr10:102115000-102115061 | Common:1; Rare:19 | ||||
chr10:102395558-102395721 | Common:1; Rare:44 | ||||
chr10:102714271-102714627 | Common:2; Rare:119 | ||||
chr10:102776078-102776228 | Common:1; Rare:23 | ||||
chr10:103396411-103396709 | Rare:106 | ||||
chr10:104338373-104338539 | Rare:46 | ||||
chr10:109923423-109923655 | Common:2; Rare:89 | ||||
chr10:110007692-110008019 | Rare:95 | ||||
chr10:110304875-110305119 | Common:2; Rare:85 | ||||
chr10:110567400-110567749 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):5 | ||||
chr10:110919329-110919632 | Common:7; Rare:82 |