The correct answer is all of the other answers are correct. H3K4me1 (Histone 3 Lysine 4 methyl 1) marks where enhancers are in the chromatin landscape. By further identifying H3K27Ac or H3K27Me3 marks on the same histone, we can determine whether the enhancer is active or inactive, respectively. A DNase 1 hypersensitivity assay will preferentially cut open chromatin, which often is indicative of enhancer regions in the chromatin landscape. 

Recombination frequencies are used to map genes on chromosomes by determining their relative distances from other genes. If a distance is large, there is a higher chance that a recombination event can occur between these two genes. Linkage occurs when genes are so close to one another that the genes always segregate together (recombination never occurs between them). The only answer that makes sense is that high recombination frequencies lead to the conclusion that two genes are far apart.

A low recombination frequency would indicate that the gene loci are close together, and a recombination frequency of zero would indicate linked genes.

The larger the recombination frequency, the larger the distance between two genes. By looking at the data, we know that genes W and X are close to one another. Also, genes X and Y are close to one another. Gene Z, however, seems to be far away from both W and Y (but closer to W). We can represent these distances relatively in a picture:

W - - - X (3)

X - - Y (2)

Y - - - - - - - - - - - - - Z (13)

Z - - - - - - - - W (8)

The most likely explanation is that W, X, and Y are close to one another and Z is located slightly farther away on whichever side W is closest. A spatial map would look something like this:

Z - - - - - - - - - - W - - - X - - Y

If the genes were linked, there would be an incredibly small recombination frequency. If the genes were on opposite ends of the chromosome or on separate chromosomes, the recombination frequency would approach the maximum of 50%.

Because the recombination frequency is relatively intermediate, we can conclude that the distance between the genes does not fall at either extreme. The genes are neither very close, nor very far apart.

Genetic linkages are determined by frequencies of recombination. These are measures of how often chromosomal crossovers will take place between two genes. The closer the loci of the two genes are on a chromosome, the less likely a crossover event will separate the two genes. If the recombination frequencies are sufficiently low, the genes are considered to be linked.

Genetic linkage has nothing to do with genes coding for the same mRNA, sharing a promoter, or overlapping one another. Linked genes still code for distinctly separate traits/proteins and have different loci (don't overlap).

Gene families consist of several copies of genes that encode very similar proteins. These likely arose due to gene duplications, and were altered by mutation over time to generate separate similar proteins. It is not a requirement that members of gene families have identical DNA or amino acid sequences. Both prokaryotes and eukaryotes have gene families.

A common example is the homeobox, or Hox, gene family, which codes for several proteins that are essential for developmental timing and orientation.

Transposable elements are portions of the DNA that are free to move around the genome and are generally considered non-coding DNA. This can be potentially dangerous, however. Transposable elements can insert themselves in the coding regions of genes, thus making them non-functional. This can lead to disease. Both eukaryotic and prokaryotic genomes contain transposable elements.

Class I transposable elements are RNA-mediated elements of a single evolutionary origin, and are found in yeast, which only have class I elements, and in eukaryotes, which have both class I and class II elements. Bacteria only have class II elements, and hence are not included in the correct answer to this question.

The only difference between most LTR retrotransposons and retroviruses are that retroviruses can encode an envelope protein. Phylogenetic analyses have shown that retrotransposons and retroviruses are extremely closely related, and may be direct ancestors of one another.

Movement of transposons is very commonly controlled by RNA interference. The RNAi system cuts up problematic RNAs, and uses these small pieces to target transposons for destruction.