Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27504085-27504421 | Rare:157; Clinvar:5; Clinvar (benign):1 | ||||
chr10:28532435-28532862 | Common:5; Rare:161 | ||||
chr10:28532989-28533194 | Rare:84 | ||||
chr10:29735773-29736098 | Common:3; Rare:70 | ||||
chr10:30059503-30059689 | Common:1; Rare:70 | ||||
chr10:30349117-30349136 | Rare:6 | ||||
chr10:30349256-30349400 | Common:12; Rare:83 | ||||
chr10:30433865-30434228 | Common:3; Rare:98 | ||||
chr10:31031846-31032052 | Common:2; Rare:83 | ||||
chr10:31319021-31319267 | Common:2; Rare:70 | ||||
chr10:31928698-31928986 | Common:4; Rare:108 | ||||
chr10:32056364-32056555 | Common:1; Rare:79 | ||||
chr10:32378663-32378890 | Common:1; Rare:30 | ||||
chr10:32446044-32446345 | Common:1; Rare:120 | ||||
chr10:32958149-32958537 | Common:3; Rare:147 |