Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:175008362-175008632 | Common:2; Rare:60 | ||||
chr1:178037884-178038042 | Rare:56 | ||||
chr1:178098281-178098499 | Common:1; Rare:31 | ||||
chr1:178542245-178542293 | Rare:6 | ||||
chr1:180561444-180561588 | Common:1; Rare:33 | ||||
chr1:181089929-181089998 | Rare:24 | ||||
chr1:183471124-183471458 | Common:2; Rare:60 | ||||
chr1:183630258-183630504 | Common:1; Rare:49 | ||||
chr1:185316221-185316387 | Rare:43 | ||||
chr1:197201240-197201556 | Common:1; Rare:107 | ||||
chr1:198937382-198937597 | Common:2; Rare:41 | ||||
chr1:201358873-201359058 | Common:1; Rare:42 | ||||
chr1:201359614-201359807 | Common:2; Rare:42; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:201362364-201362401 | Rare:10; Clinvar:2; Clinvar (benign):1 | ||||
chr1:201369704-201369778 | Common:1; Rare:24 |