Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41262381-41262628 | Rare:38 | ||||
chr19:41264951-41265109 | Common:2; Rare:34 | ||||
chr19:41310140-41310279 | Rare:59 | ||||
chr19:41353786-41354045 | Common:2; Rare:92 | ||||
chr19:41363818-41363992 | Common:1; Rare:63; Clinvar:1 | ||||
chr19:41364123-41364173 | Rare:16; Clinvar:1 | ||||
chr19:41397593-41397849 | Common:7; Rare:90; Clinvar (benign):5 | ||||
chr19:41860103-41860285 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
chr19:41884132-41884458 | Rare:84 | ||||
chr19:42075811-42076191 | Rare:106 | ||||
chr19:42132496-42132627 | Rare:29 | ||||
chr19:42220128-42220370 | Common:2; Rare:64 | ||||
chr19:42302316-42302534 | Rare:62 | ||||
chr19:42325405-42325679 | Rare:67 | ||||
chr19:42423582-42423753 | Common:1; Rare:58 |