Skip to main content
. Author manuscript; available in PMC: 2016 Dec 23.
Published in final edited form as: Birth Defects Res A Clin Mol Teratol. 2015 Aug 17;103(10):857–862. doi: 10.1002/bdra.23413

Fig. 1.

Fig. 1

Schematic genomic structure of FOXF2 and coordinates of 9 SNPs genotyped in this study and SNPs representing those genotyped using Illumina 610-Chips for NSCL/P GWAS. Variant NM_001452.1 of the human FOXF2 gene is shown in the figure with 2 exons aligned from left to right. Filled black boxes represent exons. Scale on top of the figure shows position of the gene and coordinates for the 9 SNPs (black) genotyped in this study and some of the 32 SNPs (gray) genotyped using Illumina 610-Chips in NSCL/P GWAS basing on GRCh build 38. There are 5 SNPs (rs1737753, rs10498654, rs1711969, rs1878475 and rs1711970) genotyped between rs12524544 and rs1711971 at the 5′ of the gene, and there are another 24 SNPs (rs4959557, rs1711973, rs746095, rs731394, rs9501718, rs9328051, rs11753773, rs9378623, rs1711959, rs1711960, rs9392288, rs1555110, rs1737786, rs9502924, rs11242687, rs9405475, rs2493158, rs9502928, rs1922932, rs10458124, rs7774941, rs17202895, rs9328053, rs932410) genotyped between rs6596817 and rs2816251 at the 3′ of the gene in the NSCL/P GWAS panel.