FFCP PHASE1:Hg19::chr8:124031213..124031224,-: Difference between revisions
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=NA | |EntrezGene=NA | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=no_gencodeV16_or_build2_transcript | |||
|HGNC=NA | |HGNC=NA | ||
|TSSclassifier=strong | |||
|UniProt=NA | |UniProt=NA | ||
|association_with_transcript=NA | |||
|cluster_id=chr8:124031213..124031224,- | |||
|coexpression_cluster_id=C440 | |||
|description=CAGE_peak_at_chr8:124031213..124031224,- | |||
|id=chr8:124031213..124031224,- | |||
|ontology_enrichment_celltype= | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2= | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:1240!1.84e-11!39;DOID:8692!2.67e-11!31;DOID:9119!5.28e-09!1;DOID:2531!1.69e-08!51;DOID:0060083!1.69e-08!51 | |||
|ontology_enrichment_disease_v019=DOID:8692;4.53e-08;31 | |||
|ontology_enrichment_disease_v019_2=DOID:8692,7.41e-08,31 | |||
|ontology_enrichment_uberon=UBERON:0000989!4.19e-09!1;UBERON:0008811!4.19e-09!1;UBERON:0006258!4.19e-09!1;UBERON:0005876!4.19e-09!1;UBERON:0004874!4.19e-09!1 | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p@chr8:124031213..124031224,- | |||
}} | }} |
Latest revision as of 14:33, 31 July 2015
Short description: | p@chr8:124031213..124031224, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr8:124031213..124031224, - |
Coexpression cluster: | C440_biphenotypic_acute_immature_splenic_B_myelodysplastic_Eosinophils |
Association with transcript: | NA |
EntrezGene: | NA |
HGNC: | NA |
UniProt: | NA |
Genome view: | ZENBU |
View on UCSC genome browser
CAGE Expression
- Click each plot point to find sample in table
Ontology-based sample term enrichment analysis<b>Summary:</b>This analysis has been performed by utilizing wilcoxon rank sum test.When the number of associated cells/tissues are > n , randomly sampled n cells/tissues are used for P value calculation with rank sum test. this process are repeated several times, and the P values are averaged on the log space <br><b>Analyst:</b> Hideya Kawaji<br><br>link to source dataset<br>data
Ontology term | p-value | n |
---|---|---|
myeloid leukemia | 7.41e-08 | 31 |