Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102245216-102245561 | Common:1; Rare:57 | ||||
chr10:102418722-102419081 | Rare:76 | ||||
chr10:102419091-102419235 | Rare:30 | ||||
chr10:102419666-102419838 | Rare:50 | ||||
chr10:102432546-102432766 | Common:1; Rare:64 | ||||
chr10:102461267-102461431 | Rare:48 | ||||
chr10:102502633-102503035 | Common:1; Rare:110 | ||||
chr10:102714244-102714619 | Common:2; Rare:129 | ||||
chr10:102854128-102854284 | Common:1; Rare:58 | ||||
chr10:103193240-103193349 | Common:5; Rare:39; Clinvar (benign):1 | ||||
chr10:103277013-103277138 | Rare:33 | ||||
chr10:103277428-103277946 | Common:1; Rare:136; Clinvar (pathogenic):1 | ||||
chr10:103351011-103351185 | Common:1; Rare:69 | ||||
chr10:103396417-103396693 | Rare:99 | ||||
chr10:104268960-104269190 | Common:3; Rare:54 |