Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:95301417-95301568 | Rare:39 | ||||
chr13:95676887-95677210 | Common:3; Rare:121 | ||||
chr13:96053344-96053515 | Common:2; Rare:77 | ||||
chr13:98977981-98978174 | Common:2; Rare:38 | ||||
chr13:99200668-99200914 | Common:6; Rare:116 | ||||
chr13:100088922-100089120 | Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596785-102597039 | Common:1; Rare:119 | ||||
chr13:102773736-102773860 | Rare:54 | ||||
chr13:102798945-102799136 | Common:1; Rare:42 | ||||
chr13:106567919-106568267 | Rare:94 | ||||
chr13:108218339-108218520 | Rare:71 | ||||
chr13:110307717-110307785 | Common:1; Rare:20 | ||||
chr13:110561626-110561889 | Common:5; Rare:89 | ||||
chr13:111153529-111153720 | Common:2; Rare:95 | ||||
chr13:112689755-112690041 | Common:5; Rare:98 |