Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109090665-109090814 | Common:3; Rare:28 | ||||
chr1:109236100-109236547 | Common:1; Rare:95 | ||||
chr1:109283092-109283303 | Common:1; Rare:50 | ||||
chr1:109426275-109426497 | Rare:80 | ||||
chr1:109483758-109483970 | Common:4; Rare:55 | ||||
chr1:109548507-109548839 | Common:5; Rare:116; Clinvar (pathogenic):1 | ||||
chr1:109619724-109619886 | Rare:36 | ||||
chr1:109656025-109656367 | Common:3; Rare:87 | ||||
chr1:109984828-109985167 | Common:1; Rare:102 | ||||
chr1:110003791-110004069 | Rare:52 | ||||
chr1:110004072-110004504 | Common:5; Rare:67 | ||||
chr1:110018438-110018602 | Common:1; Rare:51 | ||||
chr1:110339047-110339494 | Common:2; Rare:135 | ||||
chr1:110407592-110407851 | Common:4; Rare:107 | ||||
chr1:110963619-110963731 | Rare:37 |