Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101818397-101818762 | Common:1; Rare:97 | ||||
chr10:102056115-102056359 | Common:1; Rare:59 | ||||
chr10:102394348-102394582 | Common:1; Rare:61 | ||||
chr10:102395536-102395735 | Common:1; Rare:53 | ||||
chr10:102432556-102432835 | Common:2; Rare:81 | ||||
chr10:102714180-102714653 | Common:2; Rare:152 | ||||
chr10:102776078-102776269 | Common:1; Rare:31 | ||||
chr10:102854175-102854292 | Common:1; Rare:39 | ||||
chr10:103193243-103193433 | Common:5; Rare:61; Clinvar (benign):1 | ||||
chr10:103396411-103396709 | Rare:106 | ||||
chr10:103918117-103918551 | Common:5; Rare:115 | ||||
chr10:104121752-104122180 | Common:3; Rare:144 | ||||
chr10:104268912-104269208 | Common:3; Rare:73 | ||||
chr10:104274855-104275188 | Common:1; Rare:81 | ||||
chr10:109923429-109923660 | Common:2; Rare:88 |