Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160343181-160343398 | Rare:90 | ||||
chr1:161021111-161021237 | Common:1; Rare:37 | ||||
chr1:161038913-161039010 | Rare:37 | ||||
chr1:161045888-161046033 | Common:1; Rare:36 | ||||
chr1:161118009-161118146 | Rare:71 | ||||
chr1:161132426-161132700 | Common:1; Rare:94 | ||||
chr1:161199049-161199299 | Rare:40 | ||||
chr1:161314283-161314417 | Common:3; Rare:54; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749796-161749828 | Rare:19 | ||||
chr1:161766164-161766378 | Common:3; Rare:66 | ||||
chr1:163321752-163321845 | Rare:23 | ||||
chr1:165768772-165768938 | Common:1; Rare:74 | ||||
chr1:167935943-167936249 | Common:1; Rare:93 | ||||
chr1:167936559-167936994 | Common:1; Rare:156 | ||||
chr1:169106112-169106361 | Common:4; Rare:90 |