Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40090886-40090959 | Common:1; Rare:20 | ||||
chr19:40348388-40348720 | Common:4; Rare:108 | ||||
chr19:40576719-40576902 | Common:3; Rare:56 | ||||
chr19:40750472-40750779 | Common:2; Rare:76 | ||||
chr19:40751064-40751332 | Common:3; Rare:78 | ||||
chr19:41264964-41265110 | Common:2; Rare:31 | ||||
chr19:41363956-41363971 | Rare:4; Clinvar:1 | ||||
chr19:41364123-41364317 | Rare:61; Clinvar:1 | ||||
chr19:41397558-41397821 | Common:7; Rare:92; Clinvar (benign):4 | ||||
chr19:42075817-42076168 | Rare:91 | ||||
chr19:42302416-42302502 | Rare:19 | ||||
chr19:43754908-43755094 | Common:3; Rare:67 | ||||
chr19:43827204-43827424 | Common:2; Rare:46 | ||||
chr19:43901795-43901873 | Rare:15 | ||||
chr19:44141509-44141623 | Common:1; Rare:15 |