Enhancer ID: | E_02_103 | |
Enhancer symbol: | -- | |
Species: | Mouse | |
Position : | chr6:122700483-122702483 |
|
Biosample name: | Embryonic Stem Cell | |
Experiment class : | Low throughput |
Enhancer type: | Enhancer | |
Disease: | -- | |
DO: | -- | |
Mesh: | -- | |
Distance from TSS: | >2KB | |
Pubmed ID: | 25223790 |
Enhancer experiment: | Luciferase Reporter Assay,ChIP,ChIP-qPCR | |
Enhancer experiment description: | We also designed gRNA constructs and TALE-As to target the Nanog 5 kb upstream enhancer. Similar to the Oct4 locus, dCas9-As could bind their targeted regions and effectively activate the luciferase reporter carrying the 5 kb upstream enhancer |
Target gene : | Nanog(NANOG) | |
Strong evidence: | CRISPR/Cas9 | |
Less strong evidence: | qRT-PCR,Luciferase Reporter Assay | |
Target gene experiment description: | For Nanog luciferase assay reporter, the ~1.0 kb DNA frag_x0002_ment of the Nanog 5 kb Enhancer (?5145 to ?4154) was cloned into a mini promoter luciferase vector. |
TF name : | Klf4(EZF,GKLF)Oct4Nanog(NANOG)Sox2(ANOP3,MCOPS3) | |
TF experiment: | ChIP-seq | |
TF experiment description: | To address this possibility, we reviewed the ChIP-seq information of several pluripotency transcription factors, including KLF4,OCT4,NANOG and SOX2 at the Nanog 5kb upstream Enhancer region(42) and found that the Site 2 (targeted by both TALE and dCas9) was surrounded by the predicted KLF4 and NANOG binding sites. |
Enhancer function : | -- |
Enhancer function experiment: | -- |
Enhancer function experiment description: |
-- |
SNP ID: | -- | |
SNP position: | -- |
SNP experiment: | -- |
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