FFCP PHASE1:Hg19::chr1:246269774..246269792,-: 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=chr1:246269774..246269792,- | |||
|coexpression_cluster_id=C488 | |coexpression_cluster_id=C488 | ||
|description=CAGE_peak_at_chr1:246269774..246269792,- | |description=CAGE_peak_at_chr1:246269774..246269792,- | ||
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|ontology_enrichment_celltype=CL:0000763!2.36e-20!112;CL:0000049!2.36e-20!112;CL:0002274!5.16e-15!5;CL:0000457!5.16e-15!5;CL:0002191!5.16e-15!5;CL:0000097!5.16e-15!5;CL:0000831!5.16e-15!5;CL:0002028!5.16e-15!5;CL:0000037!5.89e-15!172;CL:0000566!5.89e-15!172;CL:0002032!1.81e-14!165;CL:0000837!1.81e-14!165;CL:0000988!8.63e-14!182;CL:0000163!2.21e-08!9 | |ontology_enrichment_celltype=CL:0000763!2.36e-20!112;CL:0000049!2.36e-20!112;CL:0002274!5.16e-15!5;CL:0000457!5.16e-15!5;CL:0002191!5.16e-15!5;CL:0000097!5.16e-15!5;CL:0000831!5.16e-15!5;CL:0002028!5.16e-15!5;CL:0000037!5.89e-15!172;CL:0000566!5.89e-15!172;CL:0002032!1.81e-14!165;CL:0000837!1.81e-14!165;CL:0000988!8.63e-14!182;CL:0000163!2.21e-08!9 | ||
|ontology_enrichment_celltype_v019=CL:0000037;1.61e-13;1!CL:0001024;1.61e-13;1!CL:0000763;3.20e-09;100 | |ontology_enrichment_celltype_v019=CL:0000037;1.61e-13;1!CL:0001024;1.61e-13;1!CL:0000763;3.20e-09;100 | ||
|ontology_enrichment_celltype_v019_2=CL:0000763,9.01e-18,108;CL:0000049,9.01e-18,108;CL:0001024,1.42e-13,1;CL:0000037,8.81e-13,168;CL:0000988,4.78e-12,177;CL:0002032,2.00e-11,161;CL:0000837,2.00e-11,161 | |||
|ontology_enrichment_development_v019= | |ontology_enrichment_development_v019= | ||
|ontology_enrichment_disease=DOID:8692!5.95e-63!31;DOID:1240!7.16e-54!39;DOID:2531!9.63e-44!51;DOID:0060083!9.63e-44!51;DOID:0050686!1.96e-15!137;DOID:162!1.80e-07!235;DOID:14566!3.36e-07!239 | |ontology_enrichment_disease=DOID:8692!5.95e-63!31;DOID:1240!7.16e-54!39;DOID:2531!9.63e-44!51;DOID:0060083!9.63e-44!51;DOID:0050686!1.96e-15!137;DOID:162!1.80e-07!235;DOID:14566!3.36e-07!239 | ||
|ontology_enrichment_disease_v019=DOID:8692;1.23e-53;31!DOID:1240;3.29e-33;39!DOID:2531;2.31e-20;51!DOID:0060083;2.31e-20;51!DOID:225;1.04e-13;1!DOID:74;1.70e-07;2 | |ontology_enrichment_disease_v019=DOID:8692;1.23e-53;31!DOID:1240;3.29e-33;39!DOID:2531;2.31e-20;51!DOID:0060083;2.31e-20;51!DOID:225;1.04e-13;1!DOID:74;1.70e-07;2 | ||
|ontology_enrichment_disease_v019_2=DOID:8692,2.16e-56,31;DOID:1240,1.43e-44,39;DOID:2531,8.81e-34,51;DOID:0060083,8.81e-34,51;DOID:225,9.73e-14,1;DOID:0050686,1.44e-11,137;DOID:74,1.64e-07,2 | |||
|ontology_enrichment_uberon= | |ontology_enrichment_uberon= | ||
|ontology_enrichment_uberon_v019= | |ontology_enrichment_uberon_v019= | ||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p@chr1:246269774..246269792,- | |short_description=p@chr1:246269774..246269792,- | ||
}} | }} |
Latest revision as of 06:04, 28 July 2015
Short description: | p@chr1:246269774..246269792, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr1:246269774..246269792, - |
Coexpression cluster: | C488_biphenotypic_acute_skeletal_hippocampus_Monocytederived_diaphragm_small |
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 | 9.01e-18 | 108 |
common myeloid progenitor | 9.01e-18 | 108 |
CD34-positive, CD38-negative hematopoietic stem cell | 1.42e-13 | 1 |
hematopoietic stem cell | 8.81e-13 | 168 |
hematopoietic cell | 4.78e-12 | 177 |
hematopoietic oligopotent progenitor cell | 2.00e-11 | 161 |
hematopoietic multipotent progenitor cell | 2.00e-11 | 161 |
Ontology term | p-value | n |
---|---|---|
myeloid leukemia | 2.16e-56 | 31 |
leukemia | 1.43e-44 | 39 |
hematologic cancer | 8.81e-34 | 51 |
immune system cancer | 8.81e-34 | 51 |
syndrome | 9.73e-14 | 1 |
organ system cancer | 1.44e-11 | 137 |
hematopoietic system disease | 1.64e-07 | 2 |