FFCP PHASE1:Hg19::chr13:90531106..90531112,+: 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=chr13:90531106..90531112,+ | |||
|coexpression_cluster_id=C439 | |||
|description=CAGE_peak_at_chr13:90531106..90531112,+ | |||
|id=chr13:90531106..90531112,+ | |||
|ontology_enrichment_celltype=CL:0000214!1.12e-17!3;CL:0000153!8.85e-07!9;CL:0000447!8.85e-07!9 | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2= | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease= | |||
|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:0006915!1.12e-17!3;UBERON:0002018!1.12e-17!3;UBERON:0002217!1.12e-17!3;UBERON:0007616!1.12e-17!3;UBERON:0004905!3.60e-11!5;UBERON:0000982!3.60e-11!5;UBERON:0004770!3.60e-11!5 | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p@chr13:90531106..90531112,+ | |||
}} | }} |
Latest revision as of 17:25, 24 July 2015
Short description: | p@chr13:90531106..90531112, + |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr13:90531106..90531112, + |
Coexpression cluster: | C439_acute_CD14_Macrophage_biphenotypic_neuroblastoma_Monocytederived_myelodysplastic |
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 |