Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:30922240-30922350 | Rare:46 | ||||
chr22:30969036-30969283 | Common:2; Rare:70 | ||||
chr22:31090285-31090623 | Common:2; Rare:55 | ||||
chr22:31100630-31101059 | Common:4; Rare:116 | ||||
chr22:31463911-31464137 | Rare:64 | ||||
chr22:36288821-36289304 | Common:2; Rare:141; Clinvar:5; Clinvar (benign):8 | ||||
chr22:36328034-36328297 | Common:1; Rare:62 | ||||
chr22:36329517-36329753 | Rare:46 | ||||
chr22:36330640-36330860 | Common:1; Rare:46 | ||||
chr22:36471072-36471218 | Common:1; Rare:26 | ||||
chr22:41092502-41092637 | Rare:70 | ||||
chr22:41413824-41414039 | Common:2; Rare:56 | ||||
chr22:41447577-41447844 | Common:1; Rare:93 | ||||
chr22:41522995-41523272 | Rare:79 | ||||
chr22:41524364-41524608 | Rare:59 |