FFCP PHASE1:Hg19::chr17:56356913..56356926,-: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=NA | |EntrezGene=NA | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=NA | |HGNC=NA | ||
|TSSclassifier=strong | |||
|UniProt=NA | |UniProt=NA | ||
|association_with_transcript=NA | |association_with_transcript=NA | ||
|cluster_id=chr17:56356913..56356926,- | |||
|coexpression_cluster_id=C209 | |||
|description=CAGE_peak_at_chr17:56356913..56356926,- | |description=CAGE_peak_at_chr17:56356913..56356926,- | ||
|id=chr17:56356913..56356926,- | |id=chr17:56356913..56356926,- | ||
|ontology_enrichment_celltype=CL:0001024!1.08e-10!1 | |ontology_enrichment_celltype=CL:0001024!1.08e-10!1 | ||
|ontology_enrichment_celltype_v019=CL:0000037;8.64e-26;1!CL:0001024;8.64e-26;1 | |||
|ontology_enrichment_celltype_v019_2=CL:0001024,7.62e-26,1 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:8692!4.79e-18!31;DOID:1240!3.84e-14!39;DOID:225!8.95e-11!1;DOID:2531!1.41e-10!51;DOID:0060083!1.41e-10!51 | |ontology_enrichment_disease=DOID:8692!4.79e-18!31;DOID:1240!3.84e-14!39;DOID:225!8.95e-11!1;DOID:2531!1.41e-10!51;DOID:0060083!1.41e-10!51 | ||
|ontology_enrichment_disease_v019=DOID:225;4.61e-26;1!DOID:8692;3.52e-20;31!DOID:74;9.40e-14;2!DOID:1240;3.13e-13;39!DOID:2531;1.11e-07;51!DOID:0060083;1.11e-07;51!DOID:1287;1.59e-07;4 | |||
|ontology_enrichment_disease_v019_2=DOID:225,4.61e-26,1;DOID:8692,3.16e-20,31;DOID:1240,3.78e-16,39;DOID:74,9.40e-14,2;DOID:2531,2.03e-12,51;DOID:0060083,2.03e-12,51;DOID:1287,1.59e-07,4 | |||
|ontology_enrichment_uberon=UBERON:0001831!1.43e-10!1;UBERON:0001567!1.43e-10!1;UBERON:0008801!1.43e-10!1;UBERON:0002581!4.75e-10!1;UBERON:0001950!6.38e-07!20;UBERON:0000200!8.98e-07!6 | |ontology_enrichment_uberon=UBERON:0001831!1.43e-10!1;UBERON:0001567!1.43e-10!1;UBERON:0008801!1.43e-10!1;UBERON:0002581!4.75e-10!1;UBERON:0001950!6.38e-07!20;UBERON:0000200!8.98e-07!6 | ||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p@chr17:56356913..56356926,- | |short_description=p@chr17:56356913..56356926,- | ||
}} | }} |
Latest revision as of 19:15, 25 July 2015
Short description: | p@chr17:56356913..56356926, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr17:56356913..56356926, - |
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 |
---|---|---|
CD34-positive, CD38-negative hematopoietic stem cell | 7.62e-26 | 1 |
Ontology term | p-value | n |
---|---|---|
syndrome | 4.61e-26 | 1 |
myeloid leukemia | 3.16e-20 | 31 |
leukemia | 3.78e-16 | 39 |
hematopoietic system disease | 9.40e-14 | 2 |
hematologic cancer | 2.03e-12 | 51 |
immune system cancer | 2.03e-12 | 51 |
cardiovascular system disease | 1.59e-07 | 4 |