Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147172297-147172353 | Rare:14 | ||||
chr1:147172420-147172786 | Common:1; Rare:94 | ||||
chr1:147225275-147225509 | Common:3; Rare:51 | ||||
chr1:148458722-148458975 | Common:2; Rare:71 | ||||
chr1:148679713-148679944 | Rare:20 | ||||
chr1:148951761-148952146 | Common:5; Rare:78 | ||||
chr1:148952264-148952475 | Common:4; Rare:74 | ||||
chr1:149103523-149103869 | Common:6; Rare:123 | ||||
chr1:149886637-149887004 | Common:2; Rare:137 | ||||
chr1:149887952-149888215 | Rare:57 | ||||
chr1:149927771-149927931 | Common:1; Rare:56; Clinvar (benign):4 | ||||
chr1:149936321-149936463 | Rare:33 | ||||
chr1:150010471-150010538 | Common:1; Rare:10 | ||||
chr1:150067649-150067876 | Rare:65 | ||||
chr1:150282285-150282596 | Common:3; Rare:63 |