Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7629520-7629836 | Common:5; Rare:113; Clinvar (benign):2 | ||||
chr19:7637007-7637143 | Common:2; Rare:47; Clinvar (benign):1 | ||||
chr19:7920240-7920360 | Rare:55 | ||||
chr19:7943629-7943988 | Rare:102 | ||||
chr19:8308297-8308645 | Common:2; Rare:109 | ||||
chr19:8321331-8321568 | Common:2; Rare:109 | ||||
chr19:8390068-8390411 | Common:1; Rare:97 | ||||
chr19:8444791-8444996 | Common:4; Rare:89 | ||||
chr19:9538588-9538728 | Common:1; Rare:39 | ||||
chr19:9621184-9621493 | Common:3; Rare:90 | ||||
chr19:9786112-9786272 | Rare:51 | ||||
chr19:9818809-9818858 | Rare:18 | ||||
chr19:9827570-9827954 | Common:2; Rare:104 | ||||
chr19:10333517-10333701 | Rare:62 | ||||
chr19:10403483-10403711 | Rare:108 |