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URL: http://ccg.vital-it.ch/snp2tfbs
Proper Citation: SNP2TFBS (RRID:SCR_016885)
Description: Collection of text files providing specific annotations for human single nucleotide polymorphisms (SNPs), namely whether they are predicted to abolish, create or change the affinity of one or several transcription factor (TF) binding sites. Used to investigate the molecular mechanisms underlying regulatory variation in the human genome. SNP2TFBS is also accessible over a web interface, enabling users to view the information provided for an individual SNP, to extract SNPs based on various search criteria, to annotate uploaded sets of SNPs or to display statistics about the frequencies of binding sites affected by selected SNPs.
Abbreviations: SNP2TFBS
Synonyms: Single Nucleotide Polymorphisms 2 Transcription Factor Binding Site, SNP2TFBS
Resource Type: web service, data or information resource, data access protocol, software resource, database
Defining Citation: PMID:27899579
Keywords: collection, regulatory, single, polymorphism, SNP, affecting, predicted, transcription, factor, binding, site, affinity, data, human, nucleotide, genome
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