Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:31720750-31721008 | Common:2; Rare:101 | ||||
chr20:32465400-32465850 | Common:2; Rare:94 | ||||
chr20:32475282-32475625 | Common:1; Rare:80 | ||||
chr20:32543640-32544011 | Common:3; Rare:102 | ||||
chr20:32560891-32561162 | Common:2; Rare:65 | ||||
chr20:32581551-32582381 | Common:16; Rare:222 | ||||
chr20:34262460-34262750 | Common:4; Rare:95 | ||||
chr20:34335832-34335995 | Rare:27 | ||||
chr20:36050792-36051088 | Common:4; Rare:163 | ||||
chr20:36175370-36175650 | Rare:52; Clinvar (benign):1 | ||||
chr20:36183101-36183513 | Common:6; Rare:177 | ||||
chr20:36271213-36271526 | Rare:97 | ||||
chr20:36606837-36607013 | Rare:78 | ||||
chr20:36632540-36632830 | Rare:127 | ||||
chr20:36677281-36677509 | Common:6; Rare:104 |