Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:148951750-148952178 | Common:5; Rare:87 | ||||
chr1:148952261-148952623 | Common:5; Rare:102 | ||||
chr1:149812363-149812560 | Rare:59 | ||||
chr1:149886618-149887004 | Common:2; Rare:147 | ||||
chr1:149887006-149887232 | Common:1; Rare:84 | ||||
chr1:149887895-149888016 | Rare:63 | ||||
chr1:149927740-149927900 | Common:1; Rare:64; Clinvar (benign):5 | ||||
chr1:149931305-149931625 | Common:1; Rare:89 | ||||
chr1:149933483-149933728 | Rare:75 | ||||
chr1:149936285-149936454 | Common:1; Rare:38 | ||||
chr1:149936711-149936947 | Common:2; Rare:56 | ||||
chr1:150010515-150010837 | Common:4; Rare:74 | ||||
chr1:150067585-150067912 | Common:1; Rare:94 | ||||
chr1:150150111-150150264 | Common:2; Rare:49 | ||||
chr1:150268362-150268495 | Rare:28 |