Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43324809-43325512 | Common:2; Rare:104 | ||||
chr1:43325556-43325878 | Common:1; Rare:47 | ||||
chr1:43326656-43326899 | Common:3; Rare:46 | ||||
chr1:43328457-43328781 | Common:1; Rare:55 | ||||
chr1:43416759-43417087 | Rare:50 | ||||
chr1:43440192-43440609 | Common:1; Rare:112; Clinvar (benign):5 | ||||
chr1:43441478-43441523 | Common:1; Rare:17; Clinvar:1; Clinvar (benign):1 | ||||
chr1:43441606-43441702 | Rare:22 | ||||
chr1:43447797-43447888 | Common:2; Rare:21; Clinvar:1; Clinvar (benign):1 | ||||
chr1:43448120-43448729 | Common:1; Rare:174; Clinvar:5; Clinvar (benign):6 | ||||
chr1:43454594-43454741 | Rare:36 | ||||
chr1:43554291-43554474 | Common:3; Rare:35 | ||||
chr1:43588892-43589164 | Rare:64 | ||||
chr1:43589716-43589790 | Rare:10 | ||||
chr1:43594279-43594557 | Common:2; Rare:45 |