Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:40636659-40637026 | Common:2; Rare:99 | ||||
chr22:40856721-40857162 | Common:3; Rare:165; Clinvar:4 | ||||
chr22:41286158-41286428 | Common:2; Rare:83 | ||||
chr22:41446501-41446543 | Rare:7 | ||||
chr22:41446768-41446980 | Rare:90 | ||||
chr22:41468633-41468743 | Common:2; Rare:35 | ||||
chr22:41468903-41469175 | Rare:85 | ||||
chr22:41621000-41621377 | Common:7; Rare:138 | ||||
chr22:41832909-41833196 | Common:3; Rare:95 | ||||
chr22:42070782-42071049 | Common:3; Rare:59 | ||||
chr22:42079517-42079812 | Common:2; Rare:87 | ||||
chr22:42090627-42091049 | Common:2; Rare:172; Clinvar (pathogenic):1 | ||||
chr22:42614858-42615244 | Common:3; Rare:158 | ||||
chr22:42960336-42960413 | Rare:11 | ||||
chr22:43812269-43812442 | Common:2; Rare:59 |