Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36605255-36605310 | Rare:15 | ||||
chr19:38899572-38899702 | Rare:40 | ||||
chr19:38930742-38930992 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391112-39391418 | Common:1; Rare:130 | ||||
chr19:39970883-39971196 | Common:5; Rare:88 | ||||
chr19:40348513-40348724 | Common:3; Rare:66 | ||||
chr19:44164972-44165125 | Common:1; Rare:34 | ||||
chr19:46601200-46601347 | Common:3; Rare:43 | ||||
chr19:48619139-48619506 | Common:1; Rare:119 | ||||
chr19:48993289-48993533 | Common:3; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
chr19:52397755-52397880 | Common:2; Rare:37 | ||||
chr19:54102676-54102885 | Common:3; Rare:54 | ||||
chr19:54115635-54115787 | Common:1; Rare:32; Clinvar:4 | ||||
chr19:54449044-54449233 | Common:2; Rare:52 | ||||
chr2:3558294-3558471 | Common:5; Rare:67 |