FFCP PHASE1:Hg19::chr1:210761148..210761159,+: 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=chr1:210761148..210761159,+ | |||
|description=CAGE_peak_at_chr1:210761148..210761159,+ | |description=CAGE_peak_at_chr1:210761148..210761159,+ | ||
|id=chr1:210761148..210761159,+ | |id=chr1:210761148..210761159,+ | ||
|ontology_enrichment_celltype=CL:0000062!9.49e-09!11;CL:0000375!9.49e-09!11;CL:0000335!9.49e-09!11;CL:0000057!5.81e-08!75;CL:0000055!1.22e-07!180;CL:0002620!2.51e-07!23 | |ontology_enrichment_celltype=CL:0000062!9.49e-09!11;CL:0000375!9.49e-09!11;CL:0000335!9.49e-09!11;CL:0000057!5.81e-08!75;CL:0000055!1.22e-07!180;CL:0002620!2.51e-07!23 | ||
|ontology_enrichment_celltype_v019=CL:0000062;6.41e-23;9!CL:0002569;1.44e-09;6 | |||
|ontology_enrichment_celltype_v019_2=CL:0000062,5.63e-19,11;CL:0000375,5.63e-19,11;CL:0000335,5.63e-19,11;CL:0002569,1.44e-09,6 | |||
|ontology_enrichment_development_v019=CL:0000335;5.63e-19;11 | |||
|ontology_enrichment_disease= | |||
|ontology_enrichment_disease_v019=DOID:17;2.66e-11;5!DOID:450;2.66e-11;5!DOID:66;2.66e-11;5!DOID:423;2.66e-11;5!DOID:0080000;2.66e-11;5!DOID:11722;2.66e-11;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,2.66e-11,5;DOID:450,2.66e-11,5;DOID:66,2.66e-11,5;DOID:423,2.66e-11,5;DOID:0080000,2.66e-11,5;DOID:11722,2.66e-11,5 | |||
|ontology_enrichment_uberon=UBERON:0000341!3.51e-08!2 | |ontology_enrichment_uberon=UBERON:0000341!3.51e-08!2 | ||
|ontology_enrichment_uberon_v019=UBERON:0001474;4.81e-12;18!UBERON:0003422;1.44e-09;6!UBERON:0004765;1.15e-08;26!UBERON:0003104;2.18e-08;7!UBERON:0009142;2.18e-08;7 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0003422,1.44e-09,6 | |||
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| ||
|short_description=p@chr1:210761148..210761159,+ | |short_description=p@chr1:210761148..210761159,+ | ||
}} | }} |
Latest revision as of 03:31, 28 July 2015
Short description: | p@chr1:210761148..210761159, + |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr1:210761148..210761159, + |
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 |
---|---|---|
osteoblast | 5.63e-19 | 11 |
osteoprogenitor cell | 5.63e-19 | 11 |
mesenchyme condensation cell | 5.63e-19 | 11 |
mesenchymal stem cell of umbilical cord | 1.44e-09 | 6 |
Ontology term | p-value | n |
---|---|---|
mesenchyme of umbilical cord | 1.44e-09 | 6 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 2.66e-11 | 5 |
myotonic disease | 2.66e-11 | 5 |
muscle tissue disease | 2.66e-11 | 5 |
myopathy | 2.66e-11 | 5 |
muscular disease | 2.66e-11 | 5 |
myotonic dystrophy | 2.66e-11 | 5 |