Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:9675045-9675180 | Common:1; Rare:39 | ||||
chr19:9818811-9818846 | Rare:11 | ||||
chr19:9827815-9827982 | Common:1; Rare:62 | ||||
chr19:9835013-9835347 | Rare:136 | ||||
chr19:10231269-10231572 | Common:2; Rare:64 | ||||
chr19:10333508-10333715 | Rare:69 | ||||
chr19:10836291-10836551 | Common:2; Rare:63 | ||||
chr19:10928578-10928768 | Common:1; Rare:46 | ||||
chr19:11089295-11089499 | Rare:29; Clinvar:8; Clinvar (pathogenic):1 | ||||
chr19:11197494-11197676 | Common:1; Rare:57 | ||||
chr19:11559210-11559374 | Common:1; Rare:53 | ||||
chr19:11738860-11739255 | Common:4; Rare:104 | ||||
chr19:11766904-11767099 | Rare:52 | ||||
chr19:11924795-11925145 | Common:6; Rare:84 | ||||
chr19:12551421-12551710 | Common:2; Rare:80 |