Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35784585-35784883 | Rare:67 | ||||
chr19:35851296-35851447 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr19:35856833-35856952 | Rare:26 | ||||
chr19:35900538-35900654 | Rare:26 | ||||
chr19:35902294-35902540 | Common:2; Rare:44 | ||||
chr19:35994970-35995265 | Common:1; Rare:77; Clinvar (benign):1 | ||||
chr19:36008425-36008586 | Rare:52; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:36008697-36008909 | Rare:55; Clinvar (benign):1 | ||||
chr19:36014147-36014563 | Common:2; Rare:118 | ||||
chr19:36032518-36032736 | Common:1; Rare:39 | ||||
chr19:36032762-36032936 | Common:3; Rare:43 | ||||
chr19:36054327-36054615 | Common:3; Rare:80 | ||||
chr19:36054753-36055059 | Common:2; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
chr19:36114788-36114992 | Common:2; Rare:82 | ||||
chr19:36115660-36115841 | Rare:44 |