Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:223992564-223992775 | Common:3; Rare:78 | ||||
chr1:228464617-228464860 | Rare:61 | ||||
chr10:2610957-2611110 | Common:1; Rare:34 | ||||
chr10:18290729-18290934 | Common:2; Rare:47 | ||||
chr10:24118335-24118552 | Rare:51 | ||||
chr10:46786780-46786876 | Rare:7 | ||||
chr10:73247247-73247362 | Rare:59 | ||||
chr10:87342323-87342408 | Common:2; Rare:25 | ||||
chr10:88939589-88939956 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr10:88941371-88941423 | Common:1; Rare:10; Clinvar:1; Clinvar (benign):2 | ||||
chr10:125023468-125023526 | Common:1; Rare:23 | ||||
chr11:1995874-1996000 | Common:1; Rare:29 | ||||
chr11:1996054-1996186 | Rare:39 | ||||
chr11:2138269-2138473 | Common:1; Rare:46 | ||||
chr11:65422688-65422804 | Common:1; Rare:36 |