Variant report
| Variant | rs73834333 |
|---|---|
| Chromosome Location | chr3:47582569-47582570 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:47577000-47583000 | Weak transcription | K562 | blood |
| 2 | chr3:47578600-47583800 | Weak transcription | Brain Germinal Matrix | brain |
| 3 | chr3:47578800-47582600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 4 | chr3:47578800-47586400 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 5 | chr3:47579200-47583000 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 6 | chr3:47579200-47583200 | Weak transcription | Brain Anterior Caudate | brain |
| 7 | chr3:47582000-47583800 | Enhancers | Cortex derived primary cultured neurospheres | brain |
| 8 | chr3:47582200-47583600 | Bivalent Enhancer | HepG2 | liver |
| 9 | chr3:47582400-47584000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 10 | chr3:47582400-47584200 | Weak transcription | Esophagus | oesophagus |
