Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:41486397-41486528 | Rare:26 | ||||
chr1:41662179-41662451 | Common:1; Rare:65 | ||||
chr1:42186492-42186531 | Rare:6 | ||||
chr1:42186826-42187002 | Common:3; Rare:37 | ||||
chr1:42190835-42190958 | Common:2; Rare:25 | ||||
chr1:42667902-42668162 | Rare:40 | ||||
chr1:42693993-42694114 | Common:1; Rare:25 | ||||
chr1:42696514-42696648 | Common:1; Rare:36 | ||||
chr1:42697531-42697751 | Common:2; Rare:29 | ||||
chr1:42699558-42699615 | Rare:6 | ||||
chr1:42752204-42752359 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:43448474-43448728 | Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
chr1:43595861-43595896 | Rare:7 | ||||
chr1:43958246-43958542 | Rare:54 | ||||
chr1:44048276-44048469 | Common:1; Rare:23 |