FFCP PHASE1:Hg19::chr3:120113167..120113185,-: 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=chr3:120113167..120113185,- | |||
|coexpression_cluster_id=C1208 | |||
|description=CAGE_peak_at_chr3:120113167..120113185,- | |description=CAGE_peak_at_chr3:120113167..120113185,- | ||
|id=chr3:120113167..120113185,- | |id=chr3:120113167..120113185,- | ||
|ontology_enrichment_celltype=CL:0000055!3.76e-14!180;CL:0000057!3.29e-08!75;CL:0002620!1.14e-07!23 | |ontology_enrichment_celltype=CL:0000055!3.76e-14!180;CL:0000057!3.29e-08!75;CL:0002620!1.14e-07!23 | ||
|ontology_enrichment_celltype_v019=CL:0002620;1.58e-14;23!CL:0000153;9.46e-07;9!CL:0000447;9.46e-07;9 | |||
|ontology_enrichment_celltype_v019_2=CL:0002620,1.63e-14,23;CL:0000057,6.99e-09,76 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019=DOID:17;1.51e-12;5!DOID:450;1.51e-12;5!DOID:66;1.51e-12;5!DOID:423;1.51e-12;5!DOID:0080000;1.51e-12;5!DOID:11722;1.51e-12;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,1.37e-12,5;DOID:450,1.37e-12,5;DOID:66,1.37e-12,5;DOID:423,1.37e-12,5;DOID:0080000,1.37e-12,5;DOID:11722,1.37e-12,5 | |||
|ontology_enrichment_uberon= | |ontology_enrichment_uberon= | ||
|ontology_enrichment_uberon_v019=UBERON:0004457;2.37e-10;9!UBERON:0000042;2.37e-10;9!UBERON:0002097;9.70e-08;41!UBERON:0002199;2.09e-07;46!UBERON:0002416;2.09e-07;46 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0002097,1.58e-10,41;UBERON:0002199,4.20e-09,46;UBERON:0002416,4.20e-09,46;UBERON:0004457,1.15e-07,12;UBERON:0000042,1.15e-07,12 | |||
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| ||
|short_description=p@chr3:120113167..120113185,- | |short_description=p@chr3:120113167..120113185,- | ||
}} | }} |
Latest revision as of 14:52, 29 July 2015
Short description: | p@chr3:120113167..120113185, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr3:120113167..120113185, - |
Coexpression cluster: | C1208_Chondrocyte_Preadipocyte_Fibroblast_umbilical_Smooth_skin_Olfactory |
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 |
---|---|---|
skin fibroblast | 1.63e-14 | 23 |
fibroblast | 6.99e-09 | 76 |
Ontology term | p-value | n |
---|---|---|
skin of body | 1.58e-10 | 41 |
integument | 4.20e-09 | 46 |
integumental system | 4.20e-09 | 46 |
cavity lining | 1.15e-07 | 12 |
serous membrane | 1.15e-07 | 12 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 1.37e-12 | 5 |
myotonic disease | 1.37e-12 | 5 |
muscle tissue disease | 1.37e-12 | 5 |
myopathy | 1.37e-12 | 5 |
muscular disease | 1.37e-12 | 5 |
myotonic dystrophy | 1.37e-12 | 5 |