Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:201071626-201072039 | Rare:86 | ||||
chr2:201451444-201451806 | Common:1; Rare:93 | ||||
chr2:201642637-201642764 | Rare:66 | ||||
chr2:201643449-201643509 | Rare:16; Clinvar:2 | ||||
chr2:201780890-201780994 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
chr2:202238494-202238615 | Rare:40 | ||||
chr2:202911908-202912291 | Common:2; Rare:105 | ||||
chr2:203238864-203239042 | Rare:68 | ||||
chr2:203239240-203239352 | Rare:42 | ||||
chr2:203328168-203328430 | Common:2; Rare:101 | ||||
chr2:206159378-206159989 | Common:4; Rare:183; Clinvar (benign):1 | ||||
chr2:206274931-206275034 | Rare:39 | ||||
chr2:206765297-206765645 | Common:3; Rare:88; Clinvar:4; Clinvar (benign):4 | ||||
chr2:207165936-207166124 | Rare:32 | ||||
chr2:207529774-207530104 | Common:3; Rare:93 |