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Fig. 2 | Clinical Epigenetics

Fig. 2

From: A targeted long-read sequencing approach questions the association of OXTR methylation with high-functioning autism

Fig. 2

shows the 5mC modification probability across the entire OXTR gene (Hg38:, chr3: 8,750,381–8,770,434, exons represented by dark blue boxes, coding region highlighted in bold in the legend below, transcription start site marked by dotted line) and its regulatory architecture (gene promoter region represented by red box, CpG island represented by green box containing 184 CpG sites and gene enhancer regions represented by gray boxes below). Thin lines in the figure show individual long reads and thick lines show the aggregated trend across all reads, color-coded by group. There were no apparent group differences across the entire OXTR gene, even when focusing on specific regulatory regions

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