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. 2018 Apr 10;19:24. doi: 10.1186/s12863-018-0611-1

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© The Author(s). 2018

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. 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. 4 — Schematic representation of the genomic region of mouse chromosome 10 at 38.74–44.34 cM and the homologous regions in human. The genomic regions of mouse chromosome 10 at 38.74–44.34 cM are syntenic to human 12q23.2 – q23.3, 19p13.3, 19p13.12, 21q22.3 and 22q13.3. White dots represent mouse genetic markers used in this study: rs259766385 and rs239646663 are the peak markers of Tpir2. Black dots represent human genetic markers: rs2374688 and rs2839235 are the single nucleotide polymorphisms associated with urinary albumin excretion and glomerular filtration rate in human, respectively [21]; and PAH and D19S591 (also known as GATA44F10) are the genetic markers associated with urinary albumin excretion in patients with essential hypertension [22]. Chr., chromosome