Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145823885-145824268 | Rare:139 | ||||
chr1:145858996-145859154 | Rare:46 | ||||
chr1:145885823-145885968 | Rare:21 | ||||
chr1:145918686-145919005 | Common:2; Rare:67 | ||||
chr1:145927433-145927648 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr1:145957991-145958195 | Rare:45 | ||||
chr1:145964615-145964743 | Rare:30 | ||||
chr1:145996469-145996852 | Common:2; Rare:152 | ||||
chr1:146228953-146229182 | Common:2; Rare:53 | ||||
chr1:147172449-147172823 | Common:1; Rare:94 | ||||
chr1:147225312-147225466 | Common:3; Rare:32 | ||||
chr1:148679755-148679912 | Rare:17 | ||||
chr1:148952271-148952609 | Common:5; Rare:101 | ||||
chr1:149390400-149390634 | Rare:32 | ||||
chr1:149812091-149812135 | Rare:16 |