Variant report
Variant | rs1348963 |
---|---|
Chromosome Location | chr11:45663473-45663474 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:45659200-45669400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr11:45663000-45666800 | Enhancers | HUVEC | blood vessel |
3 | chr11:45663400-45663600 | Enhancers | Spleen | Spleen |
4 | chr11:45663400-45666200 | Enhancers | Primary neutrophils fromperipheralblood | blood |