Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27154315-27154480 | Rare:43 | ||||
chr10:27155091-27155453 | Common:7; Rare:134; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240390-27240889 | Common:2; Rare:148 | ||||
chr10:27242058-27242248 | Common:1; Rare:84 | ||||
chr10:27743504-27743713 | Rare:58 | ||||
chr10:28532430-28532862 | Common:5; Rare:163 | ||||
chr10:28532958-28533200 | Rare:98 | ||||
chr10:28677264-28677528 | Common:5; Rare:124 | ||||
chr10:29735763-29735975 | Common:3; Rare:40 | ||||
chr10:30059505-30059655 | Common:1; Rare:58 | ||||
chr10:30433842-30434228 | Common:4; Rare:109 | ||||
chr10:30434268-30434702 | Common:2; Rare:105 | ||||
chr10:30434784-30434939 | Common:1; Rare:34 | ||||
chr10:30999417-30999649 | Rare:41 | ||||
chr10:31031820-31032067 | Common:2; Rare:98 |