Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44737259-44737776 | Common:2; Rare:80 | ||||
chr19:44753685-44753835 | Common:1; Rare:22 | ||||
chr19:44908402-44908592 | Rare:61; Clinvar (pathogenic):1 | ||||
chr19:44935970-44936201 | Common:1; Rare:55 | ||||
chr19:44943912-44944209 | Common:3; Rare:61 | ||||
chr19:45882745-45883001 | Rare:63 | ||||
chr19:46860910-46861141 | Common:1; Rare:77 | ||||
chr19:47264663-47264898 | Common:1; Rare:113 | ||||
chr19:47489712-47490054 | Common:1; Rare:86 | ||||
chr19:47863778-47863947 | Common:2; Rare:26 | ||||
chr19:47868957-47869066 | Common:2; Rare:26 | ||||
chr19:47869107-47869321 | Common:1; Rare:33 | ||||
chr19:49491486-49491794 | Common:1; Rare:101 | ||||
chr19:54162285-54162567 | Common:10; Rare:73 | ||||
chr19:55230398-55230640 | Common:3; Rare:104 |