“…One element of TE targeting comes directly from the fact that integration is restricted to open chromatin regions. This is apparent in mammalian brains, where somatic LINE insertions are enriched in the proximity of neuronal genes [11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33]. If we consider that TEs can be the target of epigenetic marks, the non-random and targeted tissue-specific distribution of TEs can be considered a mechanism to genetically fix a landmark, which could induce an epigenetic control of nearby gene expression (Figure 1B).…”