Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:31399376-31399663 | Common:1; Rare:84 | ||||
chr22:31750116-31750324 | Common:1; Rare:47 | ||||
chr22:31753759-31753982 | Rare:77 | ||||
chr22:32474636-32474985 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):2 | ||||
chr22:35257406-35257501 | Common:1; Rare:25 | ||||
chr22:35399905-35400197 | Rare:102 | ||||
chr22:35840364-35840542 | Rare:32 | ||||
chr22:36529080-36529529 | Common:6; Rare:140 | ||||
chr22:37019426-37019758 | Common:5; Rare:93 | ||||
chr22:37560324-37560529 | Common:1; Rare:68 | ||||
chr22:37849276-37849452 | Rare:109 | ||||
chr22:37953532-37953742 | Common:1; Rare:81 | ||||
chr22:38506290-38506526 | Common:1; Rare:78 | ||||
chr22:38570154-38570493 | Common:5; Rare:64 | ||||
chr22:38656328-38656687 | Common:1; Rare:98 |