Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20447646-20448015 | Common:1; Rare:105 | ||||
chr2:20448018-20448268 | Rare:87 | ||||
chr2:20448362-20448820 | Common:2; Rare:115 | ||||
chr2:20450898-20451058 | Rare:40 | ||||
chr2:21042433-21042558 | Rare:38; Clinvar:4; Clinvar (benign):1 | ||||
chr2:26191481-26191919 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr2:27025653-27025932 | Common:2; Rare:62 | ||||
chr2:28391691-28391837 | Rare:35 | ||||
chr2:28393380-28393617 | Rare:76 | ||||
chr2:28394663-28394729 | Rare:14 | ||||
chr2:28606989-28607288 | Common:1; Rare:74 | ||||
chr2:28625365-28625705 | Rare:70 | ||||
chr2:30346511-30346698 | Common:1; Rare:47 | ||||
chr2:36357608-36357672 | Common:1; Rare:14 | ||||
chr2:36537168-36537469 | Common:1; Rare:84 |