FFCP PHASE1:Hg19::chr19:823786..823802,-: 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=chr19:823786..823802,- | |||
|coexpression_cluster_id=C1114 | |coexpression_cluster_id=C1114 | ||
|description=CAGE_peak_at_chr19:823786..823802,- | |description=CAGE_peak_at_chr19:823786..823802,- | ||
|id=chr19:823786..823802,- | |id=chr19:823786..823802,- | ||
|ontology_enrichment_celltype=CL:0000763!6.73e-10!112;CL:0000049!6.73e-10!112 | |ontology_enrichment_celltype=CL:0000763!6.73e-10!112;CL:0000049!6.73e-10!112 | ||
|ontology_enrichment_celltype_v019=CL:0002032;1.83e-13;1!CL:0000037;1.83e-13;1!CL:0001024;1.83e-13;1!CL:0000557;1.83e-13;1!CL:0000763;8.62e-08;100 | |||
|ontology_enrichment_celltype_v019_2=CL:0000763,9.71e-18,108;CL:0000049,9.71e-18,108;CL:0001024,2.07e-13,1;CL:0000037,9.57e-13,168;CL:0000988,5.18e-12,177;CL:0002032,2.10e-11,161;CL:0000837,2.10e-11,161 | |||
|ontology_enrichment_development_v019=CL:0000049;1.40e-08;108 | |||
|ontology_enrichment_disease=DOID:8692!6.08e-42!31;DOID:1240!1.65e-32!39;DOID:2531!6.55e-24!51;DOID:0060083!6.55e-24!51;DOID:162!1.63e-11!235;DOID:14566!3.87e-11!239;DOID:0050686!1.23e-10!137 | |ontology_enrichment_disease=DOID:8692!6.08e-42!31;DOID:1240!1.65e-32!39;DOID:2531!6.55e-24!51;DOID:0060083!6.55e-24!51;DOID:162!1.63e-11!235;DOID:14566!3.87e-11!239;DOID:0050686!1.23e-10!137 | ||
|ontology_enrichment_disease_v019=DOID:8692;2.01e-55;31!DOID:1240;6.75e-37;39!DOID:2531;4.21e-22;51!DOID:0060083;4.21e-22;51!DOID:225;3.98e-14;1!DOID:74;1.05e-07;2 | |||
|ontology_enrichment_disease_v019_2=DOID:8692,2.62e-56,31;DOID:1240,1.67e-44,39;DOID:2531,9.91e-34,51;DOID:0060083,9.91e-34,51;DOID:225,3.98e-14,1;DOID:0050686,1.50e-11,137;DOID:74,1.05e-07,2 | |||
|ontology_enrichment_uberon= | |ontology_enrichment_uberon= | ||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p@chr19:823786..823802,- | |short_description=p@chr19:823786..823802,- | ||
}} | }} |
Latest revision as of 18:37, 27 July 2015
Short description: | p@chr19:823786..823802, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr19:823786..823802, - |
Coexpression cluster: | C1114_acute_myelodysplastic_biphenotypic_Whole_CD14_granulocyte_Reticulocytes |
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 | 9.71e-18 | 108 |
common myeloid progenitor | 9.71e-18 | 108 |
CD34-positive, CD38-negative hematopoietic stem cell | 2.07e-13 | 1 |
hematopoietic stem cell | 9.57e-13 | 168 |
hematopoietic cell | 5.18e-12 | 177 |
hematopoietic oligopotent progenitor cell | 2.10e-11 | 161 |
hematopoietic multipotent progenitor cell | 2.10e-11 | 161 |
Ontology term | p-value | n |
---|---|---|
myeloid leukemia | 2.62e-56 | 31 |
leukemia | 1.67e-44 | 39 |
hematologic cancer | 9.91e-34 | 51 |
immune system cancer | 9.91e-34 | 51 |
syndrome | 3.98e-14 | 1 |
organ system cancer | 1.50e-11 | 137 |
hematopoietic system disease | 1.05e-07 | 2 |