Variant report
Variant | rs11891596 |
---|---|
Chromosome Location | chr2:205063307-205063308 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:205056600-205068000 | Weak transcription | Aorta | Aorta |
2 | chr2:205063000-205068200 | Enhancers | Liver | Liver |
3 | chr2:205063200-205065400 | Enhancers | Primary neutrophils fromperipheralblood | blood |
4 | chr2:205063200-205065400 | Weak transcription | Cortex derived primary cultured neurospheres | brain |