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The binding elements are often occupied differently in different tissues, and these differences can be used to derive all type-specific sub-modules in silico.
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Among these cis-acting elements are often multiple GR binding sites as well as binding sites for other transcriptional regulators.
Regulatory sequence elements are often organized into defined frameworks of motifs of two or more transcription factor binding sites and clusters of such motifs.
These elements are often essential to social entrepreneurship.
Enhancer elements are often predicted from their distinctive sequence conservation.
In most carcinogenic tissue hypomethylation of repetitive elements, and particularly LINE-1 elements, is often observed.
This element is often referred to as the hormone-responsive element (HRE).
A conserved MCM single-stranded DNA binding element is essential for replication initiation.
Also, a new putative DAF-16 binding element was identified.
After ChIP assays the immediate 5′ upstream sequences containing putative NF-κB-binding elements were amplified from human genomic DNA.
However, the decisions of these bodies are not binding and are often ignored.
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