Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36397881-36398014 | Common:2; Rare:33 | ||||
chr1:36450431-36450590 | Common:1; Rare:48 | ||||
chr1:36464230-36464475 | Common:2; Rare:70 | ||||
chr1:37474409-37474587 | Rare:69 | ||||
chr1:37514734-37514843 | Rare:66 | ||||
chr1:37595888-37596029 | Common:1; Rare:44 | ||||
chr1:37692229-37692496 | Common:3; Rare:55 | ||||
chr1:37859575-37859764 | Common:3; Rare:62 | ||||
chr1:37989964-37990165 | Rare:76 | ||||
chr1:38859696-38859933 | Rare:87 | ||||
chr1:38873307-38873383 | Common:1; Rare:32 | ||||
chr1:39026174-39026397 | Common:1; Rare:55 | ||||
chr1:39691394-39691568 | Common:4; Rare:37 | ||||
chr1:39738724-39738898 | Common:2; Rare:35 | ||||
chr1:39883447-39883593 | Common:1; Rare:60; Clinvar (pathogenic):1 |