Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:200738741-200739030 | Common:6; Rare:94 | ||||
chr1:201359622-201359824 | Common:2; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:201362358-201362426 | Rare:18; Clinvar:4; Clinvar (benign):1 | ||||
chr1:201420213-201420324 | Rare:26 | ||||
chr1:201503541-201503843 | Common:4; Rare:53 | ||||
chr1:201731521-201731569 | Rare:11 | ||||
chr1:201731572-201731899 | Common:1; Rare:44 | ||||
chr1:201811670-201811955 | Rare:51 | ||||
chr1:201904644-201904880 | Common:2; Rare:32 | ||||
chr1:202810754-202811020 | Common:1; Rare:91 | ||||
chr1:202861494-202861782 | Common:1; Rare:84 | ||||
chr1:203035684-203035822 | Common:2; Rare:36 | ||||
chr1:203038314-203038607 | Common:1; Rare:42 | ||||
chr1:204288299-204288592 | Common:2; Rare:55 | ||||
chr1:204506392-204506521 | Common:4; Rare:51 |