get_read_counts: Gets read counts for a specific locus in the genome
In ctDNAtools: Analyze Circulating Tumor DNA Sequencing Data

Uses samtools pileup to get the read counts for each base in the genomic position specified

1 2	get_read_counts(chr, pos, bam, tag = "", min_base_quality = 20, max_depth = 1e+05, min_mapq = 30)

`chr`	chromosome name
`pos`	genomic coordinate
`bam`	path to bam file
`tag`	the RG tag if the bam has more than one sample
`min_base_quality`	minimum base quality for a read to be counted
`max_depth`	maximum depth above which sampling will happen
`min_mapq`	the minimum mapping quality for a read to be counted