Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151327355-151327838 | Common:4; Rare:102 | ||||
chr1:151328117-151328517 | Common:2; Rare:118 | ||||
chr1:151346838-151347073 | Rare:63 | ||||
chr1:151347208-151347572 | Rare:82 | ||||
chr1:151399380-151399596 | Common:2; Rare:63; Clinvar (pathogenic):1 | ||||
chr1:151458510-151459099 | Common:7; Rare:264 | ||||
chr1:151459162-151459271 | Rare:40 | ||||
chr1:151459460-151459793 | Rare:97 | ||||
chr1:151511204-151511431 | Common:3; Rare:51 | ||||
chr1:151539696-151539846 | Rare:25 | ||||
chr1:151540098-151540376 | Common:1; Rare:85 | ||||
chr1:151611837-151612226 | Common:3; Rare:88; Clinvar (benign):1 | ||||
chr1:151762870-151763270 | Common:6; Rare:244 | ||||
chr1:151763436-151763798 | Common:4; Rare:117 | ||||
chr1:151790422-151790874 | Common:3; Rare:110 |