Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:64252860-64252971 | Rare:21 | ||||
chr2:64257449-64257547 | Common:4; Rare:14 | ||||
chr2:64969785-64969826 | Rare:8 | ||||
chr2:67331518-67331938 | Common:2; Rare:77 | ||||
chr2:67334074-67334105 | Common:2; Rare:11 | ||||
chr2:70086262-70086485 | Common:4; Rare:90 | ||||
chr2:70088449-70088671 | Rare:46 | ||||
chr2:70125294-70125375 | Rare:31 | ||||
chr2:71416911-71417103 | Common:1; Rare:48 | ||||
chr2:74120190-74120364 | Rare:64 | ||||
chr2:74370464-74370708 | Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
chr2:76579475-76579696 | Rare:65 | ||||
chr2:77088441-77088658 | Common:7; Rare:72 | ||||
chr2:77097962-77098294 | Rare:63 | ||||
chr2:77098966-77099292 | Common:1; Rare:79 |