Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:197453267-197453554 | Rare:98 | ||||
chr2:197499795-197500424 | Common:1; Rare:240; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515835-197516087 | Common:2; Rare:93 | ||||
chr2:200509913-200510210 | Common:1; Rare:106 | ||||
chr2:200811428-200811572 | Common:1; Rare:51 | ||||
chr2:200811785-200811964 | Rare:71 | ||||
chr2:200864229-200864255 | Rare:7 | ||||
chr2:200889045-200889450 | Common:3; Rare:129 | ||||
chr2:200963594-200963897 | Common:1; Rare:77 | ||||
chr2:201071586-201072043 | Rare:101 | ||||
chr2:201117416-201117571 | Rare:17 | ||||
chr2:201118522-201118825 | Rare:47 | ||||
chr2:201451490-201451859 | Common:2; Rare:96 | ||||
chr2:201642660-201642727 | Rare:35 | ||||
chr2:201780896-201781243 | Common:3; Rare:106; Clinvar:3; Clinvar (benign):2 |