Enhancer ID: | E_01_028 | |
Enhancer symbol: | -- | |
Species: | Human | |
Position : | chr17:26072592-26074592 |
|
Biosample name: | Hep G2 | |
Experiment class : | Low throughput |
Enhancer type: | Enhancer | |
Disease: | -- | |
DO: | -- | |
Mesh: | -- | |
Distance from TSS: | >2KB | |
Pubmed ID: | 19467240 |
Enhancer experiment: | Luciferase Reporter Assay,PCR,EMSA,ChIP | |
Enhancer experiment description: | Taken together, this work identifies a far-upstream functional Oct-1 enhancer motif at -10.2 kb in the hiNOS promoter that regulates cytokine-induced hiNOS gene transcription, and further underscores the tight control mechanisms regulating expression of the human iNOS gene. |
Target gene : | NOS2(HEP-NOS,INOS,NOSA) | |
Strong evidence: | -- | |
Less strong evidence: | EMSA,ChIP | |
Target gene experiment description: | Taken together, this work identifies a far-upstream functional Oct-1 enhancer motif at -10.2 kb in the hiNOS promoter that regulates cytokine-induced hiNOS gene transcription, and further underscores the tight control mechanisms regulating expression of the human iNOS gene. |
TF name : | POU2F1(OCT1,OTF1,oct-1B) | |
TF experiment: | EMSA,ChIP | |
TF experiment description: | To examine whether the Oct-1 protein can interact with the potential Oct-1 binding site at ?10.2 kb of hiNOS in vitro, we carried out electrophoretic mobility shift assays (EMSAs) with nuclear extracts from HepG2 cells.Chromatin immunoprecipitation assay confirms that Oct-1 specifically binds to the motif at ?10.2 kb in the hiNOS promoter in vivo. |
Enhancer function : | -- |
Enhancer function experiment: | -- |
Enhancer function experiment description: |
-- |
SNP ID: | -- | |
SNP position: | -- |
SNP experiment: | -- |
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