Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32817250-32817617 | Rare:100; Clinvar:5 | ||||
chr1:33036824-33037082 | Rare:96; Clinvar (pathogenic):1 | ||||
chr1:34859676-34859884 | Common:1; Rare:54 | ||||
chr1:34985253-34985370 | Common:1; Rare:47 | ||||
chr1:35079317-35079422 | Common:3; Rare:30 | ||||
chr1:35193102-35193345 | Common:1; Rare:89 | ||||
chr1:35557377-35557481 | Common:1; Rare:23 | ||||
chr1:35557607-35557850 | Common:2; Rare:94 | ||||
chr1:35641432-35641647 | Common:1; Rare:51 | ||||
chr1:36088770-36088922 | Common:1; Rare:61 | ||||
chr1:36224097-36224493 | Common:1; Rare:123 | ||||
chr1:36450446-36450602 | Common:1; Rare:43 | ||||
chr1:36464247-36464503 | Common:3; Rare:75 | ||||
chr1:37474391-37474581 | Common:1; Rare:77 | ||||
chr1:37514736-37514855 | Common:2; Rare:72 |