Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:184664068-184664193 | Common:2; Rare:38 | ||||
chr1:185316221-185316367 | Rare:35 | ||||
chr1:197201240-197201548 | Common:1; Rare:105 | ||||
chr1:198937395-198937587 | Common:1; Rare:35 | ||||
chr1:201899186-201899261 | Common:1; Rare:17 | ||||
chr1:202563998-202564201 | Rare:36 | ||||
chr1:202810753-202810961 | Common:1; Rare:67 | ||||
chr1:203342437-203342669 | Common:1; Rare:59 | ||||
chr1:203627894-203628060 | Rare:31 | ||||
chr1:204288357-204288585 | Common:1; Rare:43 | ||||
chr1:206685587-206685713 | Rare:33 | ||||
chr1:207064579-207065089 | Common:2; Rare:119 | ||||
chr1:207326706-207326816 | Rare:32; Clinvar (pathogenic):1 | ||||
chr1:207822679-207822911 | Common:1; Rare:48 | ||||
chr1:207823965-207824128 | Common:3; Rare:24 |