Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:99279764-99279819 | Rare:6 | ||||
chr13:102394497-102394660 | Common:1; Rare:60 | ||||
chr13:105599555-105599806 | Common:3; Rare:52 | ||||
chr13:108915780-108915930 | Rare:28 | ||||
chr13:109781706-109781862 | Common:1; Rare:37 | ||||
chr13:109787614-109787781 | Common:1; Rare:42 | ||||
chr13:110174455-110174660 | Rare:73; Clinvar (benign):1 | ||||
chr13:110205351-110205540 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:110212415-110212574 | Common:1; Rare:51; Clinvar (benign):1 | ||||
chr13:110221395-110221607 | Common:1; Rare:33 | ||||
chr13:110265678-110265877 | Rare:36 | ||||
chr13:110281239-110281430 | Common:2; Rare:29 | ||||
chr13:110304261-110304523 | Common:1; Rare:41 | ||||
chr13:110308442-110308617 | Common:4; Rare:31 | ||||
chr13:110308972-110309205 | Common:3; Rare:47 |