Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:200864585-200864788 | Common:1; Rare:77 | ||||
chr2:200889005-200889439 | Common:3; Rare:141 | ||||
chr2:200963454-200963506 | Rare:8 | ||||
chr2:201071626-201072047 | Rare:86 | ||||
chr2:201451435-201451874 | Common:3; Rare:109 | ||||
chr2:201642633-201642743 | Rare:53 | ||||
chr2:201780895-201781241 | Common:3; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
chr2:202265618-202265797 | Rare:63 | ||||
chr2:202911889-202912303 | Common:2; Rare:112 | ||||
chr2:203014543-203014931 | Common:1; Rare:127 | ||||
chr2:203238779-203239050 | Common:2; Rare:97 | ||||
chr2:203239222-203239358 | Rare:48 | ||||
chr2:203535179-203535557 | Common:3; Rare:148 | ||||
chr2:205682356-205682563 | Rare:35 | ||||
chr2:205682695-205682791 | Common:1; Rare:27 |