Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17230501-17230730 | Common:1; Rare:92; Clinvar:1 | ||||
chr10:17643866-17644295 | Common:2; Rare:131 | ||||
chr10:18651553-18651756 | Common:1; Rare:87 | ||||
chr10:18659058-18659573 | Common:4; Rare:157 | ||||
chr10:21526346-21526568 | Common:1; Rare:65 | ||||
chr10:22316227-22316452 | Common:1; Rare:103 | ||||
chr10:24449557-24449692 | Rare:28 | ||||
chr10:24466408-24466633 | Rare:37 | ||||
chr10:27100427-27100628 | Common:4; Rare:59; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154315-27154480 | Rare:43 | ||||
chr10:27155139-27155409 | Common:6; Rare:102; Clinvar:5; Clinvar (benign):6 | ||||
chr10:27240478-27240667 | Common:2; Rare:58 | ||||
chr10:27240714-27240934 | Common:1; Rare:56 | ||||
chr10:27242058-27242235 | Common:1; Rare:76 | ||||
chr10:28532490-28532862 | Common:5; Rare:148 |