Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26021635-26021791 | Common:1; Rare:24 | ||||
chr1:26067607-26067829 | Common:2; Rare:33 | ||||
chr1:26279947-26280201 | Rare:141 | ||||
chr1:26306612-26306830 | Common:4; Rare:51 | ||||
chr1:26432064-26432422 | Common:5; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472292-26472627 | Common:4; Rare:122 | ||||
chr1:26787877-26788243 | Common:3; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890256-26890359 | Common:1; Rare:37 | ||||
chr1:26900060-26900205 | Rare:55 | ||||
chr1:26900428-26900568 | Rare:45 | ||||
chr1:27392417-27392669 | Common:2; Rare:83 | ||||
chr1:27672153-27672310 | Common:1; Rare:25 | ||||
chr1:27725671-27726013 | Common:3; Rare:99 | ||||
chr1:27773119-27773291 | Rare:61 | ||||
chr1:27830656-27830831 | Common:3; Rare:57 |