Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:33401489-33401601 | Rare:27 | ||||
chr20:34112102-34112448 | Rare:117 | ||||
chr20:34303335-34303550 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr20:34516282-34516451 | Common:3; Rare:68 | ||||
chr20:34558518-34558758 | Common:1; Rare:65 | ||||
chr20:35092785-35092946 | Common:1; Rare:74 | ||||
chr20:35147306-35147467 | Rare:46 | ||||
chr20:35171931-35172094 | Rare:27 | ||||
chr20:35284545-35284892 | Common:2; Rare:91 | ||||
chr20:35455059-35455310 | Common:1; Rare:88 | ||||
chr20:35664867-35665002 | Common:1; Rare:37 | ||||
chr20:35699286-35699481 | Rare:70; Clinvar (benign):3 | ||||
chr20:35742165-35742651 | Common:5; Rare:154 | ||||
chr20:36236454-36236493 | Rare:8 | ||||
chr20:36746062-36746294 | Common:2; Rare:84 |