Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32394385-32394680 | Common:1; Rare:89 | ||||
chr1:32650825-32651319 | Common:2; Rare:175 | ||||
chr1:32702611-32702876 | Rare:69 | ||||
chr1:32703561-32703687 | Rare:23 | ||||
chr1:32786089-32786417 | Common:2; Rare:64; Clinvar:1 | ||||
chr1:32817200-32817727 | Common:1; Rare:141; Clinvar:5; Clinvar (benign):3 | ||||
chr1:32817745-32817869 | Common:1; Rare:23; Clinvar (benign):1 | ||||
chr1:32818058-32818285 | Common:1; Rare:62 | ||||
chr1:32818339-32818645 | Rare:58 | ||||
chr1:33080992-33081214 | Common:2; Rare:68 | ||||
chr1:34985297-34985367 | Common:1; Rare:28 | ||||
chr1:35031235-35031414 | Common:1; Rare:36 | ||||
chr1:35031625-35032021 | Common:2; Rare:115 | ||||
chr1:35079256-35079385 | Common:1; Rare:34 | ||||
chr1:35177986-35178071 | Rare:21 |