Additional file 3 of PRDM8 reveals aberrant DNA methylation in aging syndromes and is relevant for hematopoietic and neuronal differentiation

Additional file 3: Tab. S2: Differentially methylated CpG sites in PRDM8-/- versus control. CpG sites that are either hypermethylated (1511 CpG sites) or hypomethylated (1, 738 CpG sites; delta β-value >0.2 or < -0.2) in PRDM8-/- compared to control iPSCs with β-values of the knockout and control cells, and the difference in methylation between knockout and control.

附加文件3：表S2：PRDM8基因敲除（PRDM8-/-）诱导多能干细胞（induced pluripotent stem cells, iPSCs）与对照诱导多能干细胞间的差异甲基化CpG位点。本表格收录了PRDM8-/-细胞中相较于对照组发生高甲基化（1511个CpG位点）或低甲基化（1738个CpG位点；Δβ值>0.2或<-0.2）的CpG位点，同时包含敲除细胞与对照细胞的β值，以及两组间的甲基化差异。