Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:27793692-27794045 | Rare:91 | ||||
chr19:36142654-36142942 | Rare:76 | ||||
chr19:36331740-36331967 | Common:1; Rare:51 | ||||
chr19:36797227-36797554 | Common:1; Rare:76 | ||||
chr19:38375929-38376212 | Rare:62 | ||||
chr19:39486216-39486487 | Common:2; Rare:100; Clinvar (pathogenic):1 | ||||
chr19:42396935-42397184 | Rare:59 | ||||
chr19:46860835-46861115 | Common:3; Rare:90 | ||||
chr19:48873035-48873259 | Common:2; Rare:38 | ||||
chr19:58575508-58575539 | Rare:4 | ||||
chr2:20447860-20447877 | Rare:3 | ||||
chr2:27079073-27079235 | Rare:61; Clinvar:1 | ||||
chr2:28394667-28394729 | Rare:14 | ||||
chr2:38146924-38147196 | Common:1; Rare:64 | ||||
chr2:46849922-46850192 | Rare:66 |