Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:38926608-38926921 | Common:2; Rare:94 | ||||
chr20:38962158-38962388 | Common:1; Rare:97 | ||||
chr20:40689232-40689482 | Common:1; Rare:84 | ||||
chr20:41029022-41029072 | Rare:20 | ||||
chr20:41136897-41136968 | Rare:25 | ||||
chr20:43590607-43590990 | Common:1; Rare:85 | ||||
chr20:44187050-44187373 | Common:4; Rare:76 | ||||
chr20:44187388-44187756 | Common:1; Rare:63 | ||||
chr20:44210697-44211121 | Common:5; Rare:153 | ||||
chr20:44475816-44475945 | Rare:50 | ||||
chr20:44521958-44522243 | Common:2; Rare:89 | ||||
chr20:44582108-44582366 | Common:1; Rare:44 | ||||
chr20:44582440-44582726 | Rare:39 | ||||
chr20:44651687-44651810 | Common:1; Rare:34; Clinvar (benign):1 | ||||
chr20:44714155-44714559 | Rare:66 |