Variant report
| Variant | rs3905298 |
|---|---|
| Chromosome Location | chr12:7523699-7523700 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:7506800-7527000 | Weak transcription | Placenta | Placenta |
| 2 | chr12:7520800-7526000 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 3 | chr12:7522200-7527000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 4 | chr12:7522600-7526000 | Weak transcription | K562 | blood |
| 5 | chr12:7522600-7527000 | Weak transcription | HepG2 | liver |
| 6 | chr12:7522800-7525800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 7 | chr12:7522800-7526000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 8 | chr12:7523000-7526000 | Weak transcription | NHDF-Ad | bronchial |
