MOESM3 of Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature

Additional file 3: Table S1. CpG sites showing differential methylation levels between Rahman syndrome (RMNS) and controls. Table S2. Regions showing differential methylation levels between RMNS and controls. Table S3. Classification scores generated for various blood cells. Table S4. Gene-set enrichment analysis on Reactome pathways for genes with hypomethylated regions in RMNS.

附加文件3：表S1。包含Rahman综合征（RMNS）与对照组间存在差异甲基化水平的CpG位点（CpG sites）。表S2。包含RMNS与对照组间存在差异甲基化水平的基因组区域。表S3。包含针对各类血细胞生成的分类评分。表S4。针对RMNS中携带低甲基化区域的基因，基于Reactome通路（Reactome pathways）开展的基因集富集分析（Gene-set enrichment analysis）。