FFCP PHASE1:Hg19::chr4:8437677..8437699,-: Difference between revisions
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|id=chr4:8437677..8437699,-
|short_description=p@chr4:8437677..8437699,-
|description=CAGE_peak_at_chr4:8437677..8437699,-
|association_with_transcript=NA
|EntrezG...") |
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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 | |||
|cluster_id=chr4:8437677..8437699,- | |||
|coexpression_cluster_id=C1464 | |||
|description=CAGE_peak_at_chr4:8437677..8437699,- | |||
|id=chr4:8437677..8437699,- | |||
|ontology_enrichment_celltype=CL:0000945!2.54e-18!24;CL:0000826!2.54e-18!24;CL:0000542!2.44e-14!53;CL:0000051!2.44e-14!53;CL:0000838!8.72e-13!52;CL:0000785!5.18e-08!2;CL:0000955!5.18e-08!2;CL:0000818!5.18e-08!2;CL:0000954!5.18e-08!2;CL:0000816!5.18e-08!2;CL:0002087!5.22e-07!119 | |||
|ontology_enrichment_celltype_v019=CL:0000945;5.74e-27;24!CL:0000542;6.71e-10;53 | |||
|ontology_enrichment_celltype_v019_2=CL:0000945,6.34e-27,24;CL:0000826,6.34e-27,24;CL:0000838,7.48e-13,52;CL:0000542,1.27e-12,53;CL:0000051,1.27e-12,53 | |||
|ontology_enrichment_development_v019=CL:0000051;6.71e-10;53 | |||
|ontology_enrichment_disease=DOID:0060058!6.33e-12!10 | |||
|ontology_enrichment_disease_v019=DOID:630;1.81e-40;1!DOID:0050177;1.81e-40;1!DOID:0050427;1.81e-40;1!DOID:0060058;6.65e-17;10 | |||
|ontology_enrichment_disease_v019_2=DOID:630,2.21e-40,1;DOID:0050177,2.21e-40,1;DOID:0050427,2.21e-40,1;DOID:0060058,6.39e-17,10 | |||
|ontology_enrichment_uberon=UBERON:0004177!1.89e-11!7;UBERON:0002106!1.30e-10!3;UBERON:0004854!1.30e-10!3;UBERON:0009034!1.30e-10!3;UBERON:0002095!1.30e-10!3;UBERON:0004782!1.30e-10!3;UBERON:0003281!1.30e-10!3;UBERON:0009664!1.30e-10!3;UBERON:0002296!1.30e-10!3;UBERON:0005602!1.30e-10!3;UBERON:0001179!1.30e-10!3;UBERON:0006293!1.30e-10!3 | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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| ||
|short_description=p@chr4:8437677..8437699,- | |||
}} | }} |
Latest revision as of 07:34, 30 July 2015
Short description: | p@chr4:8437677..8437699, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr4:8437677..8437699, - |
Coexpression cluster: | C1464_Burkitt_myeloma_lymphangiectasia_splenic_b_xeroderma_B |
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 |
---|---|---|
lymphocyte of B lineage | 6.34e-27 | 24 |
pro-B cell | 6.34e-27 | 24 |
lymphoid lineage restricted progenitor cell | 7.48e-13 | 52 |
lymphocyte | 1.27e-12 | 53 |
common lymphoid progenitor | 1.27e-12 | 53 |
Ontology term | p-value | n |
---|---|---|
genetic disease | 2.21e-40 | 1 |
monogenic disease | 2.21e-40 | 1 |
xeroderma pigmentosum | 2.21e-40 | 1 |
lymphoma | 6.39e-17 | 10 |