Variant report
| Variant | rs9855329 |
|---|---|
| Chromosome Location | chr3:141567355-141567356 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:141550800-141571800 | Weak transcription | Esophagus | oesophagus |
| 2 | chr3:141560200-141568200 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 3 | chr3:141560600-141572600 | Weak transcription | Spleen | Spleen |
| 4 | chr3:141564800-141570200 | Weak transcription | Placenta | Placenta |
| 5 | chr3:141565000-141572000 | Weak transcription | Adipose Nuclei | Adipose |
| 6 | chr3:141565000-141578000 | Weak transcription | Fetal Intestine Small | intestine |
| 7 | chr3:141565200-141569800 | Weak transcription | HUVEC | blood vessel |
| 8 | chr3:141566600-141568200 | Weak transcription | Lung | lung |
| 9 | chr3:141567200-141568000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 10 | chr3:141567200-141568000 | Enhancers | K562 | blood |
