Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156053756-156053921 | Rare:43 | ||||
chr1:156054611-156054910 | Common:3; Rare:83 | ||||
chr1:156061065-156061379 | Rare:68 | ||||
chr1:156082341-156082661 | Common:1; Rare:72 | ||||
chr1:156082667-156083006 | Common:1; Rare:108 | ||||
chr1:156106363-156106732 | Common:3; Rare:69 | ||||
chr1:156126108-156126203 | Rare:23; Clinvar (benign):1 | ||||
chr1:156149888-156150263 | Common:1; Rare:68 | ||||
chr1:156193832-156194129 | Common:3; Rare:78 | ||||
chr1:156212848-156213162 | Common:1; Rare:105 | ||||
chr1:156248518-156248550 | Common:1; Rare:2 | ||||
chr1:156282447-156282562 | Common:1; Rare:19 | ||||
chr1:156282786-156283043 | Common:2; Rare:59 | ||||
chr1:156295526-156295574 | Rare:11 | ||||
chr1:156338151-156338566 | Common:2; Rare:150 |