Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:204409880-204409918 | Rare:12; Clinvar:1 | ||||
chr1:204410618-204411011 | Common:1; Rare:145 | ||||
chr1:204450677-204450944 | Common:2; Rare:46 | ||||
chr1:206932454-206932883 | Rare:106 | ||||
chr1:207816646-207816967 | Common:1; Rare:59 | ||||
chr1:207822688-207822911 | Common:1; Rare:45 | ||||
chr1:209634609-209634730 | Common:1; Rare:38; Clinvar (benign):1 | ||||
chr1:211382730-211382860 | Common:1; Rare:54 | ||||
chr1:211577768-211577944 | Rare:36 | ||||
chr1:211829205-211829480 | Common:1; Rare:60 | ||||
chr1:220119068-220119330 | Rare:49 | ||||
chr1:220147337-220147514 | Rare:37; Clinvar (benign):2 | ||||
chr1:220690515-220690706 | Rare:71 | ||||
chr1:220761441-220761810 | Common:5; Rare:83 | ||||
chr1:223755260-223755545 | Rare:80 |