Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:46296745-46296925 | Rare:59 | ||||
chr22:46762517-46762693 | Common:3; Rare:62 | ||||
chr22:49918286-49918739 | Common:5; Rare:161; Clinvar (benign):3 | ||||
chr22:50525443-50525880 | Common:8; Rare:216; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
chr22:50582768-50583128 | Common:7; Rare:118; Clinvar:2; Clinvar (benign):3 | ||||
chr22:50628093-50628380 | Common:9; Rare:125; Clinvar:3; Clinvar (benign):1 | ||||
chr22:50783598-50783822 | Common:2; Rare:73 | ||||
chr3:3126810-3127093 | Common:5; Rare:114; Clinvar (benign):4 | ||||
chr3:8501558-8501920 | Common:3; Rare:139 | ||||
chr3:9363007-9363134 | Rare:42 | ||||
chr3:9397437-9397706 | Common:1; Rare:98 | ||||
chr3:9792389-9792610 | Rare:58 | ||||
chr3:9792707-9793127 | Common:3; Rare:147 | ||||
chr3:9986778-9987172 | Common:3; Rare:112 | ||||
chr3:10026292-10026425 | Rare:46 |