Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:42302430-42302454 | Rare:5 | ||||
chr19:42325405-42325675 | Rare:67 | ||||
chr19:43527155-43527310 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr19:43575465-43575713 | Common:1; Rare:76 | ||||
chr19:43580484-43580643 | Common:3; Rare:25 | ||||
chr19:43596045-43596317 | Common:3; Rare:76 | ||||
chr19:43596477-43596644 | Rare:50 | ||||
chr19:43670116-43670327 | Common:2; Rare:57 | ||||
chr19:43827204-43827433 | Common:2; Rare:48 | ||||
chr19:43901756-43901873 | Common:1; Rare:22 | ||||
chr19:44002783-44003023 | Common:4; Rare:62 | ||||
chr19:44071991-44072181 | Common:1; Rare:43 | ||||
chr19:44113137-44113451 | Common:4; Rare:72 | ||||
chr19:44141505-44141643 | Common:1; Rare:19 | ||||
chr19:44212362-44212581 | Common:4; Rare:68 |