TE insertions near known inversion breakpoints. Diagram of Chromosome 2 with the analyzed inversions. For each inversion both breakpoints, proximal (closer to the centromere) and distal (farther from the centromere), plus 2.5 kb on each side are shown. When the position of a breakpoint was not identified at the single base pair level, the interval where the breakpoint is predicted to be is shown in a gray box. Genes are shown as blue boxes, and TEs are shown as red boxes. Below each TE, the family and the number of genomes where the insertion was found/the number of genomes where the breakpoint region was identified are given. Breakpoints are shared among some of the inversions.
