Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:25016449-25016689 | Common:5; Rare:97 | ||||
chr10:26216215-26216377 | Common:1; Rare:38 | ||||
chr10:26216413-26216796 | Common:2; Rare:88 | ||||
chr10:27100409-27100630 | Common:4; Rare:63; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154315-27154495 | Rare:49 | ||||
chr10:27155216-27155423 | Common:7; Rare:94; Clinvar:2; Clinvar (benign):7 | ||||
chr10:27240496-27240601 | Rare:33 | ||||
chr10:27240605-27240666 | Common:2; Rare:16 | ||||
chr10:27240693-27240907 | Rare:56 | ||||
chr10:27242072-27242243 | Common:1; Rare:73 | ||||
chr10:27504138-27504367 | Rare:121; Clinvar:4; Clinvar (benign):1 | ||||
chr10:28532430-28532806 | Common:5; Rare:137 | ||||
chr10:30059529-30059640 | Rare:45 | ||||
chr10:31031838-31032037 | Common:1; Rare:77 | ||||
chr10:31319042-31319279 | Common:2; Rare:66 |