Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:35557353-35557470 | Rare:31 | ||||
chr1:35557642-35557839 | Common:2; Rare:74 | ||||
chr1:37474395-37474581 | Common:1; Rare:74 | ||||
chr1:37692240-37692541 | Common:4; Rare:63 | ||||
chr1:37808160-37808679 | Common:2; Rare:127 | ||||
chr1:38012524-38012799 | Rare:83 | ||||
chr1:38859717-38860033 | Rare:112 | ||||
chr1:38873296-38873407 | Common:1; Rare:44 | ||||
chr1:38941763-38941939 | Common:2; Rare:34 | ||||
chr1:40040463-40040834 | Common:3; Rare:111 | ||||
chr1:40257908-40258373 | Common:4; Rare:134; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40508666-40508747 | Rare:22 | ||||
chr1:40692015-40692199 | Common:2; Rare:65 | ||||
chr1:40979607-40979816 | Common:3; Rare:67 | ||||
chr1:42335181-42335388 | Common:5; Rare:99 |