Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:29122687-29122826 | Rare:31 | ||||
chr1:31296666-31297089 | Common:6; Rare:153 | ||||
chr1:31937771-31937889 | Rare:31 | ||||
chr1:32222326-32222481 | Rare:68 | ||||
chr1:32817258-32817686 | Rare:117; Clinvar:5; Clinvar (benign):1 | ||||
chr1:34985294-34985393 | Common:1; Rare:36 | ||||
chr1:35031643-35031820 | Rare:55 | ||||
chr1:35193109-35193183 | Rare:37 | ||||
chr1:35268627-35268998 | Rare:123 | ||||
chr1:35557369-35557485 | Common:1; Rare:27 | ||||
chr1:35557636-35557863 | Common:2; Rare:91 | ||||
chr1:37474378-37474581 | Common:1; Rare:80 | ||||
chr1:37692214-37692558 | Common:4; Rare:74 | ||||
chr1:37807627-37807809 | Rare:60 | ||||
chr1:37808153-37808541 | Common:2; Rare:102 |