FFCP PHASE1:Hg19::chr12:56736275..56736286,-: Difference between revisions
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{{FFCP|DPIdataset= | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=NA | |||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=no_gencodeV16_or_build2_transcript | |||
|HGNC=NA | |||
|TSSclassifier=strong | |||
|UniProt=NA | |||
|association_with_transcript=NA | |||
|cluster_id=chr12:56736275..56736286,- | |||
|description=CAGE_peak_at_chr12:56736275..56736286,- | |||
|id=chr12:56736275..56736286,- | |||
|ontology_enrichment_celltype= | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2= | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:14566!2.10e-18!239;DOID:162!7.09e-17!235;DOID:0050687!1.29e-13!143;DOID:0050686!1.84e-08!137;DOID:305!4.55e-08!106 | |||
|ontology_enrichment_disease_v019=DOID:630;2.88e-09;1!DOID:0050177;2.88e-09;1!DOID:4960;2.88e-09;1!DOID:0070004;2.88e-09;1!DOID:0050427;2.88e-09;1!DOID:3571;2.88e-09;1 | |||
|ontology_enrichment_disease_v019_2=DOID:630,1.56e-09,1;DOID:0050177,1.56e-09,1;DOID:0050427,1.56e-09,1;DOID:3571,1.84e-09,1;DOID:4960,5.28e-09,1;DOID:0070004,5.28e-09,1 | |||
|ontology_enrichment_uberon= | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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| |||
|short_description=p@chr12:56736275..56736286,- | |||
}} |
Latest revision as of 10:26, 24 July 2015
Short description: | p@chr12:56736275..56736286, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr12:56736275..56736286, - |
Coexpression cluster: | NA |
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 |
---|---|---|
genetic disease | 1.56e-09 | 1 |
monogenic disease | 1.56e-09 | 1 |
xeroderma pigmentosum | 1.56e-09 | 1 |
liver cancer | 1.84e-09 | 1 |
bone marrow cancer | 5.28e-09 | 1 |
myeloma | 5.28e-09 | 1 |