Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93681701-93682068 | Common:5; Rare:103 | ||||
chr1:93846571-93846817 | Common:1; Rare:88 | ||||
chr1:93847148-93847629 | Common:4; Rare:144 | ||||
chr1:93878520-93878662 | Common:1; Rare:26 | ||||
chr1:93879099-93879355 | Common:3; Rare:98 | ||||
chr1:93908821-93908918 | Common:1; Rare:16 | ||||
chr1:93909383-93909761 | Common:4; Rare:124 | ||||
chr1:94237611-94237744 | Rare:43 | ||||
chr1:94417995-94418531 | Common:3; Rare:175 | ||||
chr1:94541751-94541996 | Rare:72 | ||||
chr1:94926973-94927374 | Common:4; Rare:130 | ||||
chr1:95072575-95073048 | Common:2; Rare:169; Clinvar:2; Clinvar (benign):3 | ||||
chr1:95073228-95073363 | Common:3; Rare:30 | ||||
chr1:95233943-95234352 | Common:6; Rare:124 | ||||
chr1:96721575-96721879 | Common:2; Rare:142 |