Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:169663360-169663786 | Common:2; Rare:101 | ||||
chr3:169772748-169772808 | Rare:13 | ||||
chr3:169773068-169773418 | Common:2; Rare:112 | ||||
chr3:169966706-169966851 | Rare:61 | ||||
chr3:170908578-170908850 | Common:1; Rare:78 | ||||
chr3:173397687-173397779 | Rare:36 | ||||
chr3:177197288-177197399 | Rare:32 | ||||
chr3:179147996-179148142 | Common:1; Rare:36 | ||||
chr3:179562655-179562995 | Rare:112 | ||||
chr3:179604632-179604847 | Common:2; Rare:73 | ||||
chr3:180036739-180036798 | Rare:21 | ||||
chr3:180602048-180602366 | Common:1; Rare:109 | ||||
chr3:180989652-180989796 | Rare:62; Clinvar:1 | ||||
chr3:183099415-183099742 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr3:183635311-183635670 | Common:3; Rare:92 |