FFCP PHASE1:Hg19::chr14:70655839..70655843,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DPIdataset=robustDPI | |||
|EntrezGene=NA | |EntrezGene=NA | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=no_gencodeV16_or_build2_transcript | |||
|HGNC=NA | |HGNC=NA | ||
|TSSclassifier=W | |||
|UniProt=NA | |UniProt=NA | ||
|association_with_transcript=NA | |association_with_transcript=NA |
Revision as of 19:02, 6 July 2013
Short description: | p@chr14:70655839..70655843, + |
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Species: | Human (Homo sapiens) |
DPI dataset: | NA |
TSS-like-by-RIKEN-classifier(Yes/No): | NA |
DHS support(Yes/No): | NA |
Description: | CAGE_peak_at_chr14:70655839..70655843, + |
Coexpression cluster: | C3064_CD34_acute_Mast_Eosinophils_granulocyte_Basophils_CD133 |
Association with transcript: | NA |
EntrezGene: | NA |
HGNC: | NA |
UniProt: | NA |
Genome view: | ZENBU |
View on UCSC genome browser
CAGE Expression
Sample | p@chr14:70655839..70655843+ |
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- 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 |
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mast cell | 8.80e-63 | 5 |
basophil mast progenitor cell | 8.80e-63 | 5 |
endocrine cell | 5.71e-35 | 9 |
hematopoietic cell | 3.68e-10 | 177 |
secretory cell | 9.80e-09 | 36 |
Showing 1 to 5 of 5 entries
Ontology term | p-value | n |
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umbilical cord | 1.09e-11 | 10 |
blastocyst | 1.09e-11 | 10 |
blastula | 1.09e-11 | 10 |
bilaminar disc | 1.09e-11 | 10 |
inner cell mass | 1.09e-11 | 10 |
cleaving embryo | 1.09e-11 | 10 |
connecting stalk | 1.09e-11 | 10 |
inner cell mass derived epiblast | 1.09e-11 | 10 |
extraembryonic mesoderm | 1.09e-11 | 10 |
blood | 5.65e-08 | 15 |
Showing 1 to 10 of 14 entries
Ontology term | p-value | n |
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genetic disease | 1.10e-13 | 1 |
monogenic disease | 1.10e-13 | 1 |
xeroderma pigmentosum | 1.10e-13 | 1 |
non-Hodgkin lymphoma | 1.83e-13 | 1 |
cutaneous T cell lymphoma | 1.83e-13 | 1 |
mycosis fungoides | 1.83e-13 | 1 |
Showing 1 to 6 of 6 entries
Property "DHS support" (as page type) with input value "{{{DHSsupport}}}" contains invalid characters or is incomplete and therefore can cause unexpected results during a query or annotation process.