Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:144461629-144461716 | Common:2; Rare:40 | ||||
chr1:145823917-145824261 | Rare:120 | ||||
chr1:145858996-145859175 | Rare:51 | ||||
chr1:145918693-145918842 | Common:1; Rare:29 | ||||
chr1:145927433-145927657 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
chr1:145957961-145958212 | Rare:62 | ||||
chr1:145964587-145964749 | Rare:38 | ||||
chr1:145996562-145996748 | Rare:66 | ||||
chr1:146228991-146229182 | Common:1; Rare:35 | ||||
chr1:146938295-146938331 | Rare:16 | ||||
chr1:147172427-147172785 | Common:1; Rare:93 | ||||
chr1:147225571-147225719 | Rare:22 | ||||
chr1:147242541-147242731 | Common:3; Rare:76 | ||||
chr1:147670237-147670284 | Rare:10 | ||||
chr1:148458791-148459007 | Common:1; Rare:65 |