Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:28659737-28659818 | Rare:28 | ||||
chr13:42271382-42271524 | Common:1; Rare:45 | ||||
chr13:52194386-52194497 | Rare:35 | ||||
chr13:52617322-52617537 | Rare:52 | ||||
chr13:87671164-87671392 | Common:1; Rare:65 | ||||
chr13:100540267-100540430 | Common:1; Rare:30 | ||||
chr13:102394461-102394646 | Common:1; Rare:76 | ||||
chr13:106376435-106376625 | Common:1; Rare:38 | ||||
chr13:110205351-110205530 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:110308521-110308708 | Common:1; Rare:36 | ||||
chr13:110424741-110424996 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
chr14:22770572-22770903 | Common:2; Rare:76 | ||||
chr14:32203266-32203612 | Common:13; Rare:145 | ||||
chr14:49633956-49634076 | Common:1; Rare:48; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49862639-49862985 | Common:1; Rare:165 |