Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47256440-47256564 | Rare:41 | ||||
chr19:47484194-47484301 | Common:1; Rare:33 | ||||
chr19:48170270-48170669 | Common:2; Rare:111 | ||||
chr19:48445671-48445844 | Common:4; Rare:56 | ||||
chr19:48445914-48446019 | Rare:41 | ||||
chr19:48619139-48619598 | Common:1; Rare:153 | ||||
chr19:48810866-48811083 | Rare:72 | ||||
chr19:48900194-48900364 | Common:1; Rare:61 | ||||
chr19:48965368-48965609 | Rare:76; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:48993280-48993508 | Common:2; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
chr19:49085088-49085497 | Common:3; Rare:160 | ||||
chr19:49335335-49335380 | Rare:7 | ||||
chr19:49335382-49335774 | Common:3; Rare:119 | ||||
chr19:49336925-49337220 | Rare:94 | ||||
chr19:49453094-49453311 | Common:1; Rare:69 |