Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94025390-94025750 | Rare:73 | ||||
chr1:94063340-94063670 | Rare:71 | ||||
chr1:94237551-94237850 | Rare:96 | ||||
chr1:94418094-94418473 | Common:3; Rare:136 | ||||
chr1:94541753-94542011 | Rare:73 | ||||
chr1:94820000-94820420 | Common:4; Rare:101 | ||||
chr1:94820444-94820638 | Common:4; Rare:54 | ||||
chr1:94926050-94926450 | Common:4; Rare:150 | ||||
chr1:94927056-94927249 | Common:1; Rare:67 | ||||
chr1:95072600-95073069 | Common:4; Rare:167; Clinvar:2; Clinvar (benign):3 | ||||
chr1:95116760-95116919 | Rare:32 | ||||
chr1:95117183-95117366 | Rare:52 | ||||
chr1:95233947-95234253 | Common:5; Rare:95 | ||||
chr1:96721557-96721856 | Common:2; Rare:139 | ||||
chr1:97920902-97921180 | Common:1; Rare:112; Clinvar:3; Clinvar (pathogenic):1 |