FFCP PHASE1:Hg19::chr19:847897..847908,+: 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=chr19:847897..847908,+ | |||
|coexpression_cluster_id=C209 | |coexpression_cluster_id=C209 | ||
|description=CAGE_peak_at_chr19:847897..847908,+ | |description=CAGE_peak_at_chr19:847897..847908,+ | ||
|id=chr19:847897..847908,+ | |id=chr19:847897..847908,+ | ||
|ontology_enrichment_celltype=CL:0001024!3.08e-12!1;CL:0000763!1.44e-08!112;CL:0000049!1.44e-08!112 | |ontology_enrichment_celltype=CL:0001024!3.08e-12!1;CL:0000763!1.44e-08!112;CL:0000049!1.44e-08!112 | ||
|ontology_enrichment_celltype_v019=CL:0002032;4.59e-23;1!CL:0000557;4.59e-23;1 | |||
|ontology_enrichment_celltype_v019_2=CL:0000763,8.93e-10,108;CL:0000049,8.93e-10,108 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:8692!4.25e-28!31;DOID:1240!3.99e-22!39;DOID:2531!1.14e-16!51;DOID:0060083!1.14e-16!51;DOID:225!7.89e-13!1;DOID:74!4.83e-07!2 | |ontology_enrichment_disease=DOID:8692!4.25e-28!31;DOID:1240!3.99e-22!39;DOID:2531!1.14e-16!51;DOID:0060083!1.14e-16!51;DOID:225!7.89e-13!1;DOID:74!4.83e-07!2 | ||
|ontology_enrichment_disease_v019=DOID:8692;1.26e-25;31!DOID:225;1.34e-23;1!DOID:1240;6.36e-17;39!DOID:74;1.65e-12;2!DOID:2531;4.63e-12;51!DOID:0060083;4.63e-12;51!DOID:1287;6.87e-07;4 | |||
|ontology_enrichment_disease_v019_2=DOID:8692,1.46e-25,31;DOID:225,1.34e-23,1;DOID:1240,2.38e-20,39;DOID:2531,1.39e-15,51;DOID:0060083,1.39e-15,51;DOID:74,1.65e-12,2;DOID:1287,6.87e-07,4 | |||
|ontology_enrichment_uberon=UBERON:0002084!2.46e-12!1;UBERON:0002082!2.46e-12!1;UBERON:0004706!2.46e-12!1;UBERON:0004177!4.57e-07!7 | |ontology_enrichment_uberon=UBERON:0002084!2.46e-12!1;UBERON:0002082!2.46e-12!1;UBERON:0004706!2.46e-12!1;UBERON:0004177!4.57e-07!7 | ||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p@chr19:847897..847908,+ | |short_description=p@chr19:847897..847908,+ | ||
}} | }} |
Latest revision as of 18:40, 27 July 2015
Short description: | p@chr19:847897..847908, + |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr19:847897..847908, + |
Coexpression cluster: | C209_acute_myelodysplastic_CD34_granulocyte_CD133_liver_spleen |
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 |
---|---|---|
myeloid cell | 8.93e-10 | 108 |
common myeloid progenitor | 8.93e-10 | 108 |
Ontology term | p-value | n |
---|---|---|
myeloid leukemia | 1.46e-25 | 31 |
syndrome | 1.34e-23 | 1 |
leukemia | 2.38e-20 | 39 |
hematologic cancer | 1.39e-15 | 51 |
immune system cancer | 1.39e-15 | 51 |
hematopoietic system disease | 1.65e-12 | 2 |
cardiovascular system disease | 6.87e-07 | 4 |