Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102056100-102056327 | Common:1; Rare:55 | ||||
chr10:102114944-102115088 | Common:2; Rare:48 | ||||
chr10:102132882-102133060 | Rare:39 | ||||
chr10:102152100-102152406 | Common:3; Rare:99 | ||||
chr10:102394324-102394570 | Rare:68 | ||||
chr10:102395482-102395735 | Common:1; Rare:65 | ||||
chr10:102432546-102432820 | Common:2; Rare:78 | ||||
chr10:102714195-102714643 | Common:2; Rare:148 | ||||
chr10:102776078-102776279 | Common:1; Rare:34 | ||||
chr10:102869443-102869551 | Common:5; Rare:24 | ||||
chr10:103193240-103193548 | Common:5; Rare:84; Clinvar (benign):1 | ||||
chr10:103396411-103396719 | Rare:106 | ||||
chr10:103452262-103452431 | Rare:52 | ||||
chr10:103918120-103918540 | Common:5; Rare:114 | ||||
chr10:104268956-104269171 | Common:3; Rare:48 |