FFCP PHASE1:Hg19::chr22:39843128..39843135,+: 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=chr22:39843128..39843135,+ | |||
|coexpression_cluster_id=C342 | |coexpression_cluster_id=C342 | ||
|description=CAGE_peak_at_chr22:39843128..39843135,+ | |description=CAGE_peak_at_chr22:39843128..39843135,+ | ||
|id=chr22:39843128..39843135,+ | |id=chr22:39843128..39843135,+ | ||
|ontology_enrichment_celltype=CL:0000037!1.43e-11!172;CL:0000566!1.43e-11!172;CL:0002032!5.55e-11!165;CL:0000837!5.55e-11!165;CL:0000988!1.10e-10!182;CL:0000945!1.95e-08!24;CL:0000826!1.95e-08!24;CL:0002127!3.01e-07!1;CL:0000914!3.01e-07!1;CL:0000911!3.01e-07!1;CL:0000814!3.01e-07!1;CL:0002042!3.01e-07!1;CL:0002039!3.01e-07!1;CL:0002040!3.01e-07!1;CL:0002041!3.01e-07!1;CL:0000763!3.90e-07!112;CL:0000049!3.90e-07!112 | |ontology_enrichment_celltype=CL:0000037!1.43e-11!172;CL:0000566!1.43e-11!172;CL:0002032!5.55e-11!165;CL:0000837!5.55e-11!165;CL:0000988!1.10e-10!182;CL:0000945!1.95e-08!24;CL:0000826!1.95e-08!24;CL:0002127!3.01e-07!1;CL:0000914!3.01e-07!1;CL:0000911!3.01e-07!1;CL:0000814!3.01e-07!1;CL:0002042!3.01e-07!1;CL:0002039!3.01e-07!1;CL:0002040!3.01e-07!1;CL:0002041!3.01e-07!1;CL:0000763!3.90e-07!112;CL:0000049!3.90e-07!112 | ||
|ontology_enrichment_celltype_v019=CL:0000945;2.06e-19;24 | |||
|ontology_enrichment_celltype_v019_2=CL:0000945,2.00e-19,24;CL:0000826,2.00e-19,24;CL:0000838,1.78e-09,52;CL:0000542,2.59e-09,53;CL:0000051,2.59e-09,53 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:2531!2.42e-11!51;DOID:0060083!2.42e-11!51;DOID:8692!1.42e-10!31;DOID:1240!2.24e-10!39;DOID:630!1.46e-07!1;DOID:0050177!1.46e-07!1;DOID:0050427!1.46e-07!1;DOID:9119!3.40e-07!1;DOID:8552!5.78e-07!1 | |ontology_enrichment_disease=DOID:2531!2.42e-11!51;DOID:0060083!2.42e-11!51;DOID:8692!1.42e-10!31;DOID:1240!2.24e-10!39;DOID:630!1.46e-07!1;DOID:0050177!1.46e-07!1;DOID:0050427!1.46e-07!1;DOID:9119!3.40e-07!1;DOID:8552!5.78e-07!1 | ||
|ontology_enrichment_disease_v019=DOID:630;3.10e-50;1!DOID:0050177;3.10e-50;1!DOID:0050427;3.10e-50;1 | |||
|ontology_enrichment_disease_v019_2=DOID:630,1.46e-50,1;DOID:0050177,1.46e-50,1;DOID:0050427,1.46e-50,1 | |||
|ontology_enrichment_uberon=UBERON:0004177!9.98e-08!7 | |ontology_enrichment_uberon=UBERON:0004177!9.98e-08!7 | ||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p@chr22:39843128..39843135,+ | |short_description=p@chr22:39843128..39843135,+ | ||
}} | }} |
Latest revision as of 21:24, 28 July 2015
Short description: | p@chr22:39843128..39843135, + |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr22:39843128..39843135, + |
Coexpression cluster: | C342_xeroderma_b_B_splenic_plasma_Burkitt_thymus |
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 | 2.00e-19 | 24 |
pro-B cell | 2.00e-19 | 24 |
lymphoid lineage restricted progenitor cell | 1.78e-09 | 52 |
lymphocyte | 2.59e-09 | 53 |
common lymphoid progenitor | 2.59e-09 | 53 |
Ontology term | p-value | n |
---|---|---|
genetic disease | 1.46e-50 | 1 |
monogenic disease | 1.46e-50 | 1 |
xeroderma pigmentosum | 1.46e-50 | 1 |