Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10399269-10399411 | Common:1; Rare:28 | ||||
chr1:10399795-10399957 | Common:4; Rare:39 | ||||
chr1:10430345-10430514 | Common:3; Rare:53 | ||||
chr1:10430621-10430998 | Common:6; Rare:109 | ||||
chr1:10471879-10471999 | Rare:24 | ||||
chr1:10472047-10472347 | Common:1; Rare:57 | ||||
chr1:10472447-10472779 | Rare:77 | ||||
chr1:10474836-10475244 | Common:1; Rare:135; Clinvar:4; Clinvar (benign):1 | ||||
chr1:10475375-10475428 | Common:1; Rare:11 | ||||
chr1:10693633-10693863 | Rare:58 | ||||
chr1:10693980-10694038 | Common:1; Rare:14 | ||||
chr1:10694422-10694574 | Rare:46 | ||||
chr1:10694633-10695003 | Common:3; Rare:114 | ||||
chr1:10796640-10796860 | Common:1; Rare:61 | ||||
chr1:10975895-10976014 | Common:1; Rare:13 |