Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1324600-1324813 | Common:2; Rare:119 | ||||
chr1:2391688-2391868 | Rare:64 | ||||
chr1:7961457-7961767 | Common:4; Rare:106; Clinvar:2; Clinvar (benign):3 | ||||
chr1:9943370-9943472 | Common:2; Rare:16 | ||||
chr1:17618169-17618352 | Common:2; Rare:38 | ||||
chr1:19251512-19251830 | Common:6; Rare:102 | ||||
chr1:23980256-23980479 | Rare:73 | ||||
chr1:25232466-25232642 | Rare:68 | ||||
chr1:25819905-25820009 | Common:1; Rare:26 | ||||
chr1:26279847-26280156 | Rare:172 | ||||
chr1:26921522-26921810 | Common:3; Rare:85 | ||||
chr1:31296752-31297054 | Common:4; Rare:94 | ||||
chr1:32817294-32817577 | Rare:66; Clinvar:4 | ||||
chr1:35557357-35557470 | Rare:27 | ||||
chr1:37514747-37514828 | Rare:56 |