Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74503939-74504260 | Common:2; Rare:64 | ||||
chr2:162071188-162071335 | Rare:31 | ||||
chr2:171517733-171517907 | Common:5; Rare:27 | ||||
chr2:187003181-187003232 | Common:1; Rare:13 | ||||
chr2:188994553-188994828 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr2:188996173-188996487 | Common:12; Rare:71; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr2:189001393-189001545 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
chr2:234495922-234495986 | Rare:20 | ||||
chr22:20702728-20702866 | Common:1; Rare:24 | ||||
chr22:30246079-30246191 | Common:1; Rare:18 | ||||
chr3:49357222-49357254 | Rare:9 | ||||
chr3:52693778-52694088 | Rare:70 | ||||
chr3:80770330-80770641 | Common:7; Rare:73 | ||||
chr3:107240606-107240746 | Rare:60 | ||||
chr3:139373399-139373678 | Rare:51 |