Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927422-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964573-145964742 | Rare:43 | ||||
chr1:146228968-146229167 | Common:2; Rare:46 | ||||
chr1:147172427-147172785 | Common:1; Rare:93 | ||||
chr1:148844276-148844558 | Rare:17 | ||||
chr1:148952264-148952688 | Common:5; Rare:111 | ||||
chr1:149812166-149812269 | Rare:46 | ||||
chr1:149812278-149812532 | Common:2; Rare:115 | ||||
chr1:149842747-149842962 | Rare:3 | ||||
chr1:149850848-149851062 | Rare:1 | ||||
chr1:149886621-149887176 | Common:3; Rare:219 | ||||
chr1:149887820-149888215 | Rare:128 | ||||
chr1:149927757-149927906 | Common:1; Rare:61; Clinvar (benign):5 | ||||
chr1:149936840-149936992 | Rare:34 | ||||
chr1:150010697-150010938 | Common:1; Rare:69 |