Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:188994040-188994332 | Common:1; Rare:82; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
chr2:189004068-189004373 | Rare:91; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):20 | ||||
chr2:202036331-202036378 | Rare:13 | ||||
chr2:202297590-202297906 | Common:1; Rare:76 | ||||
chr2:202376003-202376225 | Common:3; Rare:103 | ||||
chr2:202913393-202913581 | Common:2; Rare:39 | ||||
chr2:206084375-206084667 | Common:1; Rare:62 | ||||
chr2:212270600-212270806 | Rare:32 | ||||
chr2:212498343-212498554 | Common:3; Rare:39 | ||||
chr2:214684226-214684481 | Common:1; Rare:31 | ||||
chr2:215399257-215399448 | Common:1; Rare:60 | ||||
chr2:218402614-218402714 | Rare:37 | ||||
chr2:231514362-231514555 | Common:5; Rare:76 | ||||
chr2:231712191-231712556 | Common:1; Rare:108 | ||||
chr2:236337543-236337864 | Common:4; Rare:58 |