Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:76885505-76885826 | Common:1; Rare:115 | ||||
chr13:95083823-95084097 | Common:3; Rare:34 | ||||
chr13:98976028-98976162 | Common:1; Rare:26 | ||||
chr13:98992502-98992691 | Rare:48 | ||||
chr13:110205351-110205532 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:110212415-110212574 | Common:1; Rare:51; Clinvar (benign):1 | ||||
chr13:110307826-110308123 | Common:1; Rare:111 | ||||
chr13:110308515-110308622 | Common:1; Rare:21 | ||||
chr13:110409539-110409829 | Common:3; Rare:46 | ||||
chr13:110870188-110870566 | Common:3; Rare:57 | ||||
chr14:33564779-33565040 | Common:1; Rare:57 | ||||
chr14:38254565-38254912 | Rare:118 | ||||
chr14:49633949-49634110 | Common:1; Rare:77; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49862645-49862948 | Common:1; Rare:150 | ||||
chr14:61751057-61751219 | Rare:40 |