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. 2018 May 8;19:334. doi: 10.1186/s12864-018-4718-6

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© The Author(s) 2018

Open Access This 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. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 5 — Genomic variation distributions. Distributions of multiple types of variants across the Jurkat genome. Plotted data listed from outside-in: 1. hg19 genome ideogram (gray); 2. Density of SnpEff “High Impact” SNVs with rare ExAC allele frequencies (gold); 3. Homozygous deletions that lie in coding exons (red); 4. Deletions longer than 25 kb (blue); 5. Insertions longer than 50 bp that lie in coding exons (green); 6. Inversions longer than 25 kb (cyan); 7. Interchromosomal translocations (center)