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. 2011 May 26;6(5):e17711. doi: 10.1371/journal.pone.0017711

Figure 1. The genomic structure of MCHR1 and the analyzed region.

Figure 1

(I) Genomic structure of MCHR1. MCHR1 is located on chromosome 22q13.2 and shown according to NM_005297. Boxes represent the two exons of MCHR1; white parts show untranslated regions (UTRs) and green parts show coding regions (CDS). Three potential translation start sites are indicated by black triangles. The SNPs rs133072 and rs133073 are located in the coding region of the first exon. (II) Detailed view of the analyzed region. White circles indicate CpGs. Alleles of SNPs rs133072 and rs133073 are highlighted in green. Red asterisks mark the potential methylation site created by one allele of either SNP. In our data set, only the two haplotypes GT and AC were observed.