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The occurrence of SNVs in human genomic regions. (A) Preference of SNV occurrence in PQS region versus in the entire genome. (B) Enrichment of SNVs in PQS regions. (C) The overlap frequency of SNV and PQS over genome intervals around TSS. (D) Total G4Vs caused by SNVs in the human genome. (E) The occurrence of G4V across human Refseq genes. (F) Three-dimensional presentation of G4V occurrence across human Refseq genes sorted in descending order by the mean of G4V frequency.
