FFCP PHASE2:Hg19::chr11:68049967..68049992,+
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| Short description: | p@chr11:68049967..68049992, + |
|---|---|
| Species: | Human (Homo sapiens) |
| DPI dataset: | Robust |
| TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
| DHS support(Yes/No): | Yes |
| Description: | CAGE_peak_at_chr11:68049967..68049992, + |
| Coexpression cluster: | C69_anaplastic_CD14_cord_hairy_mycosis_adult_NK |
| Association with transcript: | NA |
| EntrezGene: | NA |
| HGNC: | NA |
| UniProt: | NA |
| Genome view: | ZENBU |
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CAGE Expression
| Sample | p@chr11:68049967..68049992+ |
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- 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 lineage restricted progenitor cell | 1.14e-24 | 66 |
| granulocyte monocyte progenitor cell | 2.79e-24 | 67 |
| classical monocyte | 7.93e-24 | 42 |
| CD14-positive, CD16-negative classical monocyte | 7.93e-24 | 42 |
| myeloid leukocyte | 1.72e-22 | 72 |
| defensive cell | 1.10e-20 | 48 |
| phagocyte | 1.10e-20 | 48 |
| myeloid cell | 1.72e-19 | 108 |
| common myeloid progenitor | 1.72e-19 | 108 |
| mast cell | 2.32e-19 | 5 |
Showing 1 to 10 of 24 entries
| Ontology term | p-value | n |
|---|---|---|
| bone marrow | 3.16e-21 | 76 |
| bone element | 1.48e-19 | 82 |
| skeletal element | 1.14e-17 | 90 |
| immune system | 4.78e-17 | 93 |
| hematopoietic system | 4.34e-16 | 98 |
| blood island | 4.34e-16 | 98 |
| skeletal system | 9.85e-16 | 100 |
| hemolymphoid system | 1.95e-14 | 108 |
| musculoskeletal system | 1.13e-08 | 167 |
| lateral plate mesoderm | 8.71e-07 | 203 |
Showing 1 to 10 of 10 entries
| Ontology term | p-value | n |
|---|---|---|
| genetic disease | 9.61e-12 | 1 |
| monogenic disease | 9.61e-12 | 1 |
| xeroderma pigmentosum | 9.61e-12 | 1 |
Showing 1 to 3 of 3 entries
