Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927430-145927644 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958223 | Rare:53 | ||||
chr1:145964567-145964742 | Rare:45 | ||||
chr1:145996518-145996808 | Rare:114 | ||||
chr1:146228952-146229156 | Common:3; Rare:53 | ||||
chr1:146938294-146938336 | Rare:18 | ||||
chr1:147172427-147172779 | Common:1; Rare:91 | ||||
chr1:147541264-147541583 | Common:1; Rare:53 | ||||
chr1:148458795-148459006 | Common:1; Rare:63 | ||||
chr1:148679711-148679944 | Rare:20 | ||||
chr1:148952222-148952673 | Common:5; Rare:113 | ||||
chr1:149812073-149812152 | Rare:38 | ||||
chr1:149812184-149812579 | Common:2; Rare:167 | ||||
chr1:149813687-149813804 | Common:2; Rare:39 | ||||
chr1:149842748-149842928 | Rare:3 |