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. 2022 Oct;32(10):1930–1940. doi: 10.1101/gr.276770.122

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© 2022 Yu et al.; Published by Cold Spring Harbor Laboratory Press

This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see https://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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Figure 2. — Description of built-in genomic features: replication origins and others. (A) Landscape view of replication origins on human chromosomes. (B) Distribution of width/length of replication origins. (C) Distribution of inter-origin distance. Long, barren intervals appear as outliers in the whole-data set view (All). Thus, we excluded the outliers and showed the distance boxplot for the mass component (Mass). (D) Nucleotide base content in (−2 k, 2 k) flanking regions of replication origins. (E) Nucleotide base content in (−2 k, 2 k) flanking regions of transcription start sites (TSSs). (F) Nucleotide base content in (−2 k, 2 k) flanking regions of enhancers. (G) Nucleotide base content in (−2 k, 2 k) flanking regions of retrotransposon insertion polymorphism (RIP) sites.