Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20350828-20351092 | Common:2; Rare:115 | ||||
chr2:20446841-20447076 | Common:3; Rare:95 | ||||
chr2:20651031-20651280 | Rare:76 | ||||
chr2:20823045-20823134 | Rare:37 | ||||
chr2:23927067-23927333 | Common:3; Rare:94 | ||||
chr2:23940379-23940577 | Common:4; Rare:66 | ||||
chr2:24076225-24076594 | Rare:101 | ||||
chr2:24123262-24123508 | Common:1; Rare:66 | ||||
chr2:24972036-24972145 | Common:1; Rare:30 | ||||
chr2:25252222-25252502 | Rare:60 | ||||
chr2:25878445-25878657 | Common:1; Rare:62 | ||||
chr2:26033774-26034238 | Common:4; Rare:169 | ||||
chr2:26244593-26244984 | Common:2; Rare:143; Clinvar:5; Clinvar (benign):8 | ||||
chr2:26345798-26346184 | Common:1; Rare:115 | ||||
chr2:26764193-26764357 | Common:2; Rare:64 |