Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:144461558-144461716 | Common:5; Rare:70 | ||||
chr1:145823922-145824083 | Rare:61 | ||||
chr1:145824086-145824251 | Rare:52 | ||||
chr1:145918684-145919013 | Common:2; Rare:71 | ||||
chr1:145927394-145927644 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958223 | Rare:52 | ||||
chr1:145964573-145964747 | Rare:44 | ||||
chr1:145996572-145996868 | Common:1; Rare:110 | ||||
chr1:146228968-146229126 | Common:2; Rare:44 | ||||
chr1:147172427-147172779 | Common:1; Rare:91 | ||||
chr1:148152304-148152345 | Rare:17 | ||||
chr1:148458820-148459006 | Common:1; Rare:56 | ||||
chr1:148679530-148679859 | Rare:28 | ||||
chr1:148952557-148952673 | Common:1; Rare:16 | ||||
chr1:149103513-149103712 | Common:5; Rare:79 |