FFCP PHASE1:Hg19::chr11:33676379..33676397,+: 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 | |association_with_transcript=NA | ||
|cluster_id=chr11:33676379..33676397,+ | |||
|coexpression_cluster_id=C359 | |||
|description=CAGE_peak_at_chr11:33676379..33676397,+ | |description=CAGE_peak_at_chr11:33676379..33676397,+ | ||
|id=chr11:33676379..33676397,+ | |id=chr11:33676379..33676397,+ | ||
|ontology_enrichment_celltype=CL:0000945!5.51e-27!24;CL:0000826!5.51e-27!24;CL:0000946!5.62e-19!1;CL:0000786!5.62e-19!1;CL:0000980!5.62e-19!1;CL:0000838!2.00e-12!52;CL:0000542!3.45e-12!53;CL:0000051!3.45e-12!53;CL:0001014!2.72e-10!2;CL:0001016!2.72e-10!2;CL:0000785!3.58e-10!2;CL:0000955!3.58e-10!2;CL:0000818!3.58e-10!2;CL:0000954!3.58e-10!2;CL:0000816!3.58e-10!2;CL:0000817!3.35e-07!3;CL:0002031!9.51e-07!124 | |ontology_enrichment_celltype=CL:0000945!5.51e-27!24;CL:0000826!5.51e-27!24;CL:0000946!5.62e-19!1;CL:0000786!5.62e-19!1;CL:0000980!5.62e-19!1;CL:0000838!2.00e-12!52;CL:0000542!3.45e-12!53;CL:0000051!3.45e-12!53;CL:0001014!2.72e-10!2;CL:0001016!2.72e-10!2;CL:0000785!3.58e-10!2;CL:0000955!3.58e-10!2;CL:0000818!3.58e-10!2;CL:0000954!3.58e-10!2;CL:0000816!3.58e-10!2;CL:0000817!3.35e-07!3;CL:0002031!9.51e-07!124 | ||
|ontology_enrichment_celltype_v019=CL:0000945;1.01e-09;24 | |||
|ontology_enrichment_celltype_v019_2=CL:0000945,1.01e-09,24;CL:0000826,1.01e-09,24 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:630!8.95e-20!1;DOID:0050177!8.95e-20!1;DOID:0050427!8.95e-20!1 | |ontology_enrichment_disease=DOID:630!8.95e-20!1;DOID:0050177!8.95e-20!1;DOID:0050427!8.95e-20!1 | ||
|ontology_enrichment_disease_v019=DOID:630;5.42e-195;1!DOID:0050177;5.42e-195;1!DOID:0050427;5.42e-195;1 | |||
|ontology_enrichment_disease_v019_2=DOID:630,5.42e-195,1;DOID:0050177,5.42e-195,1;DOID:0050427,5.42e-195,1 | |||
|ontology_enrichment_uberon=UBERON:0002372!1.30e-19!1;UBERON:0001961!1.30e-19!1;UBERON:0001744!1.30e-19!1;UBERON:0001735!1.30e-19!1;UBERON:0002370!7.41e-19!4;UBERON:0005058!7.41e-19!4;UBERON:0009113!7.41e-19!4;UBERON:0003295!7.41e-19!4;UBERON:0005562!7.41e-19!4;UBERON:0001042!7.29e-17!10;UBERON:0009145!7.29e-17!10;UBERON:0006562!2.15e-15!11;UBERON:0003351!6.50e-13!6;UBERON:0004177!3.30e-11!7;UBERON:0001557!3.52e-09!19;UBERON:0000974!4.04e-08!10;UBERON:0003408!4.04e-08!10;UBERON:0009722!1.84e-07!11;UBERON:0007690!1.84e-07!11 | |ontology_enrichment_uberon=UBERON:0002372!1.30e-19!1;UBERON:0001961!1.30e-19!1;UBERON:0001744!1.30e-19!1;UBERON:0001735!1.30e-19!1;UBERON:0002370!7.41e-19!4;UBERON:0005058!7.41e-19!4;UBERON:0009113!7.41e-19!4;UBERON:0003295!7.41e-19!4;UBERON:0005562!7.41e-19!4;UBERON:0001042!7.29e-17!10;UBERON:0009145!7.29e-17!10;UBERON:0006562!2.15e-15!11;UBERON:0003351!6.50e-13!6;UBERON:0004177!3.30e-11!7;UBERON:0001557!3.52e-09!19;UBERON:0000974!4.04e-08!10;UBERON:0003408!4.04e-08!10;UBERON:0009722!1.84e-07!11;UBERON:0007690!1.84e-07!11 | ||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p@chr11:33676379..33676397,+ | |short_description=p@chr11:33676379..33676397,+ | ||
}} | }} |
Latest revision as of 21:39, 23 July 2015
Short description: | p@chr11:33676379..33676397, + |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr11:33676379..33676397, + |
Coexpression cluster: | C359_xeroderma_tonsil_acute_colon_lymph_trachea_bladder |
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 |
---|---|---|
lymphocyte of B lineage | 1.01e-09 | 24 |
pro-B cell | 1.01e-09 | 24 |
Ontology term | p-value | n |
---|---|---|
genetic disease | 5.42e-195 | 1 |
monogenic disease | 5.42e-195 | 1 |
xeroderma pigmentosum | 5.42e-195 | 1 |