Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93846506-93846745 | Common:1; Rare:69 | ||||
chr1:93847220-93847286 | Common:1; Rare:14 | ||||
chr1:93879088-93879274 | Common:1; Rare:70 | ||||
chr1:93909506-93909693 | Common:1; Rare:71 | ||||
chr1:94418216-94418472 | Common:2; Rare:89 | ||||
chr1:94541751-94541994 | Rare:72 | ||||
chr1:94820186-94820375 | Common:3; Rare:48 | ||||
chr1:94926981-94927492 | Common:4; Rare:168 | ||||
chr1:95072878-95073008 | Rare:51 | ||||
chr1:95233945-95234236 | Common:5; Rare:86 | ||||
chr1:96721579-96721867 | Common:2; Rare:136 | ||||
chr1:97920877-97921122 | Rare:92; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:98661598-98661863 | Common:1; Rare:94 | ||||
chr1:99850006-99850154 | Common:1; Rare:58 | ||||
chr1:99850325-99850389 | Rare:18; Clinvar:1 |