Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:79405779-79405880 | Rare:38 | ||||
chr13:79406227-79406314 | Common:1; Rare:27 | ||||
chr13:94601568-94601924 | Common:4; Rare:106 | ||||
chr13:95301417-95301580 | Rare:43 | ||||
chr13:95676894-95677200 | Common:3; Rare:112 | ||||
chr13:96053351-96053568 | Common:2; Rare:93 | ||||
chr13:98977882-98978199 | Common:2; Rare:68 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:100088901-100089117 | Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596804-102597053 | Common:1; Rare:120; Clinvar (benign):1 | ||||
chr13:102798970-102799134 | Rare:34 | ||||
chr13:108218293-108218520 | Common:1; Rare:84 | ||||
chr13:110713023-110713266 | Common:2; Rare:105 | ||||
chr13:110914757-110914796 | Rare:18 | ||||
chr13:111153619-111153842 | Common:2; Rare:87 |