Enhancer ID: | E_01_112 | |
Enhancer symbol: | -- | |
Species: | Human | |
Position : | chr17:69108466-69108765 |
|
Biosample name: | LNCaP | |
Experiment class : | Low throughput |
Enhancer type: | Enhancer | |
Disease: | -- | |
DO: | -- | |
Mesh: | -- | |
Distance from TSS: | >2KB | |
Pubmed ID: | 22665440 |
Enhancer experiment: | Luciferase Reporter Assay,ChIP,3C-qPCR,ChIP-qPCR | |
Enhancer experiment description: | To determine if the rs1859962 PCa risk LD block harbors enhancers, we examined the H3K4me1 ge_x0002_nome-wide distribution defined by ChIP-seq assays in LNCaP and VCaP PCa cells.We show that there are five enhancers within the target genomic segment, hereafter referred to as E1–E5. |
Target gene : | SOX9(CMD1,CMPD1,SRA1,SRXX2,SRXY10) | |
Strong evidence: | -- | |
Less strong evidence: | qPCR | |
Target gene experiment description: | This chromatin loop was confirmed through TaqMan probe–based qPCR assays with a probe targeting the SOX9 gene (Fig. 2C). The chromatin interaction was further confirmed by sequencing the PCR product (Supplemental Fig. S7). Further_x0002_more, this chromatin loop appears to be specific to SOX9, because no other loop could be detected between E1 and any other genes(MAP2K6, KCNJ16, KCNJ2) found within this ;3-Mb window. |
TF name : | AR(AIS8,DHTR,HUMARA,HYSP1,KD,NR3C4,SBMA,SMAX1,TFM,AR)FOXA1(HNF3A,TCF3A) | |
TF experiment: | ChIP,Luciferase Reporter Assay | |
TF experiment description: | In agreement, the luciferase assay in LNCaP cells depletedor not of AR using siRNA reveals that AR is required for the increased transcriptional response associated with the rs8072254 variant A allele.The FKH PWM, defined based on thousands of FOXA1 binding sites identified by ChIP-seq assays, reveals that the tenth position is invariably an A residue. |
Enhancer function : | -- |
Enhancer function experiment: | -- |
Enhancer function experiment description: |
-- |
SNP ID: | rs1859961 | |
SNP position: | 69108655 |
SNP experiment: | Luciferase Reporter Assay,ChIP |
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