Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147541213-147541572 | Common:2; Rare:56 | ||||
chr1:148458870-148458967 | Common:1; Rare:31 | ||||
chr1:148951851-148952043 | Common:2; Rare:45 | ||||
chr1:148952213-148952603 | Common:5; Rare:109 | ||||
chr1:149812192-149812547 | Common:2; Rare:162 | ||||
chr1:149842736-149842919 | Rare:3 | ||||
chr1:149850848-149851062 | Rare:1 | ||||
chr1:149886600-149887172 | Common:3; Rare:224 | ||||
chr1:149887864-149888215 | Rare:109 | ||||
chr1:149927734-149927900 | Common:1; Rare:65; Clinvar (benign):5 | ||||
chr1:150067649-150067873 | Rare:65 | ||||
chr1:150235811-150236039 | Common:2; Rare:38 | ||||
chr1:150236041-150236396 | Common:1; Rare:85 | ||||
chr1:150257719-150257915 | Rare:40 | ||||
chr1:150258036-150258123 | Rare:18 |