Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32650908-32651322 | Common:2; Rare:151 | ||||
chr1:32817250-32817758 | Common:1; Rare:140; Clinvar:5; Clinvar (benign):3 | ||||
chr1:32885757-32886006 | Rare:25 | ||||
chr1:32893310-32893492 | Rare:33 | ||||
chr1:33036806-33037105 | Rare:113; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081217 | Common:3; Rare:69 | ||||
chr1:33392737-33392963 | Rare:31 | ||||
chr1:33472377-33472673 | Rare:65 | ||||
chr1:34985301-34985400 | Common:1; Rare:35 | ||||
chr1:35031645-35031783 | Rare:46 | ||||
chr1:35079308-35079422 | Common:3; Rare:32 | ||||
chr1:35192554-35192723 | Common:1; Rare:56 | ||||
chr1:35193092-35193440 | Common:2; Rare:117 | ||||
chr1:35268663-35269049 | Rare:146 | ||||
chr1:35557353-35557481 | Common:1; Rare:36 |