FFCP PHASE1:Hg19::chr7:131195751..131195762,+: 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=chr7:131195751..131195762,+ | |||
|coexpression_cluster_id=C1090 | |||
|description=CAGE_peak_at_chr7:131195751..131195762,+ | |description=CAGE_peak_at_chr7:131195751..131195762,+ | ||
|id=chr7:131195751..131195762,+ | |id=chr7:131195751..131195762,+ | ||
|ontology_enrichment_celltype=CL:0002322!8.39e-14!5;CL:0002139!1.68e-08!24;CL:0005020!3.08e-07!6;CL:0002138!3.08e-07!6;CL:0005022!3.08e-07!6 | |ontology_enrichment_celltype=CL:0002322!8.39e-14!5;CL:0002139!1.68e-08!24;CL:0005020!3.08e-07!6;CL:0002138!3.08e-07!6;CL:0005022!3.08e-07!6 | ||
|ontology_enrichment_celltype_v019=CL:0002620;1.20e-13;23!CL:0002322;6.55e-08;5 | |||
|ontology_enrichment_celltype_v019_2=CL:0002620,1.10e-13,23;CL:0002322,7.49e-08,5 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease= | |||
|ontology_enrichment_disease_v019=DOID:17;3.11e-27;5!DOID:450;3.11e-27;5!DOID:66;3.11e-27;5!DOID:423;3.11e-27;5!DOID:0080000;3.11e-27;5!DOID:11722;3.11e-27;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,2.08e-27,5;DOID:450,2.08e-27,5;DOID:66,2.08e-27,5;DOID:423,2.08e-27,5;DOID:0080000,2.08e-27,5;DOID:11722,2.08e-27,5 | |||
|ontology_enrichment_uberon= | |ontology_enrichment_uberon= | ||
|ontology_enrichment_uberon_v019=UBERON:0001896;2.59e-12;3!UBERON:0005290;2.59e-12;3!UBERON:0002097;4.80e-07;41!UBERON:0002298;8.48e-07;6 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0001896,2.59e-12,3;UBERON:0005290,2.59e-12,3;UBERON:0010096,2.59e-12,3;UBERON:0002097,5.32e-08,41;UBERON:0002199,3.33e-07,46;UBERON:0002416,3.33e-07,46;UBERON:0002298,8.48e-07,6 | |||
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| ||
|short_description=p@chr7:131195751..131195762,+ | |short_description=p@chr7:131195751..131195762,+ | ||
}} | }} |
Latest revision as of 06:11, 31 July 2015
Short description: | p@chr7:131195751..131195762, + |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr7:131195751..131195762, + |
Coexpression cluster: | C1090_teratocarcinoma_Fibroblast_glioblastoma_kidney_H9_iPS_Amniotic |
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 | 1.10e-13 | 23 |
embryonic stem cell | 7.49e-08 | 5 |
Ontology term | p-value | n |
---|---|---|
medulla oblongata | 2.59e-12 | 3 |
myelencephalon | 2.59e-12 | 3 |
future myelencephalon | 2.59e-12 | 3 |
skin of body | 5.32e-08 | 41 |
integument | 3.33e-07 | 46 |
integumental system | 3.33e-07 | 46 |
brainstem | 8.48e-07 | 6 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 2.08e-27 | 5 |
myotonic disease | 2.08e-27 | 5 |
muscle tissue disease | 2.08e-27 | 5 |
myopathy | 2.08e-27 | 5 |
muscular disease | 2.08e-27 | 5 |
myotonic dystrophy | 2.08e-27 | 5 |