Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:174248452-174248779 | Common:1; Rare:106 | ||||
chr2:174395616-174395897 | Common:2; Rare:88 | ||||
chr2:174682842-174682968 | Common:1; Rare:50 | ||||
chr2:174847546-174847724 | Rare:40 | ||||
chr2:175005261-175005291 | Rare:7 | ||||
chr2:175005333-175005456 | Common:2; Rare:41 | ||||
chr2:175168100-175168562 | Common:2; Rare:122 | ||||
chr2:175181518-175181846 | Common:5; Rare:105 | ||||
chr2:176002263-176002416 | Common:2; Rare:60 | ||||
chr2:177212422-177212820 | Common:4; Rare:160 | ||||
chr2:177216709-177216947 | Rare:78 | ||||
chr2:177263498-177263709 | Common:1; Rare:58 | ||||
chr2:177264604-177264826 | Common:2; Rare:69 | ||||
chr2:177392638-177392840 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
chr2:177552739-177552829 | Rare:37 |