Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37514665-37514824 | Common:1; Rare:82 | ||||
chr1:37595894-37595977 | Common:1; Rare:30 | ||||
chr1:37690464-37690713 | Common:6; Rare:71 | ||||
chr1:37692235-37692577 | Common:4; Rare:81 | ||||
chr1:37859556-37859764 | Common:3; Rare:69 | ||||
chr1:37989961-37990173 | Rare:78 | ||||
chr1:38859696-38859957 | Rare:101 | ||||
chr1:38873301-38873554 | Common:3; Rare:87 | ||||
chr1:39026245-39026397 | Common:1; Rare:41 | ||||
chr1:39268278-39268494 | Rare:35 | ||||
chr1:39691369-39691568 | Common:4; Rare:41 | ||||
chr1:39738749-39739011 | Common:3; Rare:71 | ||||
chr1:39883439-39883599 | Common:1; Rare:66; Clinvar (pathogenic):1 | ||||
chr1:40040444-40040791 | Common:3; Rare:102 | ||||
chr1:40097234-40097277 | Rare:20; Clinvar (benign):1; Clinvar (pathogenic):2 |