Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:18141061-18141114 | Rare:8 | ||||
chr10:18651553-18651737 | Common:1; Rare:77 | ||||
chr10:18659101-18659483 | Common:3; Rare:122 | ||||
chr10:19816270-19816496 | Common:5; Rare:40 | ||||
chr10:21526377-21526581 | Common:1; Rare:65 | ||||
chr10:22321528-22321686 | Rare:42 | ||||
chr10:23095338-23095629 | Rare:55 | ||||
chr10:24208848-24209151 | Rare:80 | ||||
chr10:24239456-24239464 | |||||
chr10:24722704-24722842 | Rare:37 | ||||
chr10:27100427-27100633 | Common:4; Rare:60; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154322-27154476 | Rare:42 | ||||
chr10:27155181-27155416 | Common:7; Rare:101; Clinvar:4; Clinvar (benign):7 | ||||
chr10:27240474-27240679 | Common:2; Rare:64 | ||||
chr10:27240700-27240902 | Rare:56 |