I assume you want all genes in a given locus. First, download the latest release of the appropriate GTF. You don't need the binary genome. This is what you can do using bash shell:

• Download and install bedtools. Then load it.
• Use "grep" to extract the genes only. "grep -e $'\tgene\t' /path/to/hg19.gtf > /path/to/hg19_genes.gtf"
• Convert the bed file to the correct format: chr\tstart\tstop\tname with regex if necessary. Output this to Genes.tsv.
• Then do bedtools intersect. "bedtools intersect -a /path/to/genes.tsv -b /path/to/hg19_genes.gtf -wao -bed | tr -d '"' | tr ';' '\t' > intersect.bed
• Cut out the necessary columns. Include strandedness, which I don't think I included. GTFs only use forward coordinates and you'll need to take the reverse compliment of those specified sequences. "cut -f 1-4,6,13,14,18 intersect.bed | tr ' ' '\t' > present_genes.tsv"
• For other objectives, you may need to concatenate the regions in the files to get contiguous regions, which I'm unfortunately not allowed to help you with.
• You will most likely have to customize these commands. 'gene' which is in the same column as 'CDS', 'start_codon', 'exon', etc., may be called something else. You should also read the documentation for bedtools to find out what's going on. Good luck.