The figure below shows the normalized copy number [log2(copy_number/2)] at
the selected GWAS
SNP location. The blue line denotes the average
copy
number of all normal samples, while the red line
denotes the average copy number of the corresponding tumor samples. Data source:
TCGA-LGG copy
number segmentation.
Significant results:
Data source: TCGA-LGG genotypes and gene expression data
Note: "Other groups combined" = non-"IDH-mutant only" and non-"Triple-Positive" samples.
Select a molecular group:
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{{ col }}
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Select target gene:
(Submit above) is
the homozygous risk genotype group. The eQTL results are displayed for the queried LD
SNP.
The table below shows all ChIP-seq peaks from ENCODE covering the
queried LD SNP location. The ENCODE_ID links to the corresponding
experiment page on the ENCODE website. Data source: ChIP-seq peaks from ENCODE
The table below shows a list of candidate transcription factors (TFs)
whose binding affinity was significantly disrupted by the queried LD SNP. Column
permPvalue displays the permutation test p-value for testing the significance of
motif disruption. Note: if there are no candidate TFs from our
analysis, then no results will be displayed below. Data source: Motifs
from JASPAR2016, HOCOMOCOv10, Jolma2013 and TRANSFAC databases
The columns in the heatmap are the genotype groups with the
homozygous risk group highlighted in red. The rows are the putative transcription factors
(TFs) from motif analysis (see the left tab). Note: if there are no
candidate TFs from our
analysis then no results will be displayed below. Data source:
TCGA-LGG gene expression data