Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:45374040-45374303 | Common:6; Rare:94 | ||||
chr10:45727116-45727316 | Common:3; Rare:79 | ||||
chr10:45972352-45972564 | Common:1; Rare:69 | ||||
chr10:46030526-46030724 | Common:1; Rare:63 | ||||
chr10:49941919-49942133 | Rare:65 | ||||
chr10:50067817-50068008 | Common:5; Rare:85 | ||||
chr10:50623364-50623512 | Common:2; Rare:30 | ||||
chr10:50623876-50624084 | Common:1; Rare:82 | ||||
chr10:50624886-50624976 | Common:1; Rare:35 | ||||
chr10:50739855-50739964 | Rare:25 | ||||
chr10:50991094-50991373 | Common:4; Rare:79 | ||||
chr10:51074402-51074691 | Common:1; Rare:67; Clinvar (benign):7 | ||||
chr10:51699545-51699638 | Common:1; Rare:39 | ||||
chr10:58268924-58269295 | Common:6; Rare:120 | ||||
chr10:58385343-58385499 | Common:1; Rare:50 |