Enhancer ID: | E_01_288 | |
Enhancer symbol: | HGE(HER2 gene body Enhancer ) | |
Species: | Human | |
Position : | chr17:37879571-37880263 |
|
Biosample name: | K-562 | |
Experiment class : | Low throughput |
Enhancer type: | Enhancer | |
Disease: | Breast Cancer | |
DO: | DOID:1612 | |
Mesh: | D001943 | |
Distance from TSS: | Intron | |
Pubmed ID: | 29035388 |
Enhancer experiment: | DNaseI-seq,ChIP-PCR,ChIP,Luciferase Reporter Assay | |
Enhancer experiment description: | With the ENCODE Regulation Super-track Settings, DNase I hypersensitivity sites, H3K4me1 and H3K27ac were found in the previously identified intron 1 enhancer.Chromatin immunoprecipitation (ChIP)-PCR amplicons are shown. NC: sequences to which nonspecific controls were generated. |
Target gene : | ERBB2(CD340,HER-2,HER-2/neu,HER2,MLN19,NEU,NGL,TKR1) | |
Strong evidence: | -- | |
Less strong evidence: | ChIP,Luciferase Reporter Assay | |
Target gene experiment description: | Chromatin immunoprecipitation of TFAP2C, H3K4me1 and H3K27ac were performed in SKBR3 cells and TFAP2C occupancies were confirmed at promoters 1 and 2, the intron 1 enhancer and HE.We tested the ability of the HGE to regulate the transcriptional activities of the HER2 promoters by luciferase reporter assay in 293T, SKBR3 and BT474 cells (Figure 2a). |
TF name : | TFAP2C(AP2-GAMMA,ERF1,TFAP2G,hAP-2g) | |
TF experiment: | CRISPR/Cas9 | |
TF experiment description: | The transcriptional activities of these constructs were analyzed using the luciferase assay in 293T and SKBR3 cells.We next carried out genomic editing using CRISPR-Cas9 system to determine the role of the TFAP2C-binding sites at the HGE in the regulation of HER2 expression. |
Enhancer function : | -- |
Enhancer function experiment: | -- |
Enhancer function experiment description: |
-- |
SNP ID: | -- | |
SNP position: | -- |
SNP experiment: | -- |
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