Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37690502-37690736 | Common:5; Rare:57 | ||||
chr1:37692204-37692545 | Common:4; Rare:72 | ||||
chr1:37808176-37808299 | Rare:31 | ||||
chr1:37859541-37859817 | Common:4; Rare:98 | ||||
chr1:37989961-37990129 | Rare:67 | ||||
chr1:38859662-38859945 | Rare:115 | ||||
chr1:38873286-38873564 | Common:3; Rare:93 | ||||
chr1:39026223-39026398 | Common:1; Rare:45 | ||||
chr1:39738785-39738903 | Common:1; Rare:22 | ||||
chr1:40039869-40040272 | Common:4; Rare:83 | ||||
chr1:40040444-40040830 | Common:3; Rare:117 | ||||
chr1:40161231-40161409 | Common:1; Rare:48 | ||||
chr1:40257908-40258303 | Common:4; Rare:108; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40374600-40374698 | Common:8; Rare:23 | ||||
chr1:40508647-40508812 | Common:4; Rare:46 |