Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9752617-9752893 | Common:5; Rare:47 | ||||
chr2:9801748-9801971 | Common:1; Rare:41 | ||||
chr2:19933439-19933644 | Common:3; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:20447729-20447732 | Rare:1 | ||||
chr2:20447860-20447972 | Rare:36 | ||||
chr2:28378203-28378212 | Rare:2 | ||||
chr2:54571045-54571185 | Common:2; Rare:25 | ||||
chr2:55282202-55282345 | Common:4; Rare:48 | ||||
chr2:62698867-62698901 | Rare:6 | ||||
chr2:70552594-70552709 | Common:1; Rare:24 | ||||
chr2:70617708-70617860 | Rare:28 | ||||
chr2:71050051-71050221 | Common:3; Rare:28 | ||||
chr2:73981340-73981694 | Rare:67 | ||||
chr2:87455158-87455520 | Common:1; Rare:64 | ||||
chr2:88016539-88016817 | Common:10; Rare:119 |