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. 2015 Oct 13;60:1722–1733. doi: 10.1007/s11434-015-0905-x

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© Science China Press and Springer-Verlag Berlin Heidelberg 2015

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Fig. 1 — Estimated proportions of various selected genomic features within the human genome. Annotations were taken from GENCODE v23 with duplicate exons removed, and the UCSC genome browser “repeats and variations/rmsk” track for the human hg38 (GRCh38.p3) assembly. Base-pair numbers add up to greater than the sequenced genome size as some regions of DNA can overlap (e.g., lncRNAs and TEs, genes and TEs, antisense transcripts, and alternate splice sites). Consequently, the annotated features are somewhat overestimated and the unannotated genome underestimated