Schema for Watson - James Watson (CSHL) (from Human Mar. 2006 assembly)
Database: hg19    Primary Table: pgWatson    Row Count: 2,059,384
Format description: personal genome SNP
fieldexampleSQL type description
bin 585smallint(5) unsigned A field to speed indexing
chrom chr1varchar(255) Chromosome
chromStart 52057int(10) unsigned Start position in chrom
chromEnd 52058int(10) unsigned End position in chrom
name G/Cvarchar(255) alleles
alleleCount 2int(11) number of alleles
alleleFreq 2,2varchar(255) comma separated list of frequency of each allele
alleleScores 0,0varchar(255) comma separated list of quality scores
Sample Rows
binchromchromStartchromEndnamealleleCountalleleFreqalleleScores
585chr15205752058G/C22,20,0
585chr15223752238G110
585chr15554455545T130
585chr15638056381T/C21,40,0
585chr15795157952C110
585chr15821058211G110
585chr15877058771T/C210,20,0
585chr16144161442G120
585chr16326763268T/C21,10,0
585chr16951069511G110

Note: all start coordinates in our database are 0-based, not 1-based. See explanation here.