Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151165840-151166171 | Common:3; Rare:93 | ||||
chr1:151195072-151195419 | Common:2; Rare:75 | ||||
chr1:151198384-151198628 | Common:2; Rare:89 | ||||
chr1:151254624-151254801 | Rare:44 | ||||
chr1:151281925-151282318 | Rare:115 | ||||
chr1:151327663-151327791 | Rare:27 | ||||
chr1:151346854-151347049 | Rare:53 | ||||
chr1:151399480-151399635 | Common:2; Rare:59; Clinvar (pathogenic):2 | ||||
chr1:151540137-151540361 | Common:1; Rare:74 | ||||
chr1:151763457-151763557 | Common:1; Rare:35 | ||||
chr1:151790481-151790845 | Common:2; Rare:78 | ||||
chr1:151909382-151909709 | Common:4; Rare:118 | ||||
chr1:151993750-151993994 | Common:4; Rare:88 | ||||
chr1:152036912-152037091 | Common:2; Rare:49 | ||||
chr1:152908355-152908550 | Common:1; Rare:30 |