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1 ##fileformat=VCFv4.0
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2 ##fileDate=20090805
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3 ##source=myImputationProgramV3.1
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4 ##reference=1000GenomesPilot-NCBI36
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5 ##phasing=partial
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6 ##INFO=<ID=NS,Number=1,Type=Integer,Description="Number of Samples With Data">
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7 ##INFO=<ID=AN,Number=1,Type=Integer,Description="Total number of alleles in called genotypes">
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8 ##INFO=<ID=AC,Number=.,Type=Integer,Description="Allele count in genotypes, for each ALT allele, in the same order as listed">
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9 ##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
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10 ##INFO=<ID=AF,Number=.,Type=Float,Description="Allele Frequency">
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11 ##INFO=<ID=AA,Number=1,Type=String,Description="Ancestral Allele">
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12 ##INFO=<ID=DB,Number=0,Type=Flag,Description="dbSNP membership, build 129">
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13 ##INFO=<ID=H2,Number=0,Type=Flag,Description="HapMap2 membership">
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14 ##FILTER=<ID=q10,Description="Quality below 10">
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15 ##FILTER=<ID=s50,Description="Less than 50% of samples have data">
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16 ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
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17 ##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
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18 ##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
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19 ##FORMAT=<ID=HQ,Number=2,Type=Integer,Description="Haplotype Quality">
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20 ##ALT=<ID=DEL:ME:ALU,Description="Deletion of ALU element">
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21 ##ALT=<ID=CNV,Description="Copy number variable region">
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22 ##sampling="random sampling using vcfrandomsample -p 1 -r 0.2 /space/anton/galaxy-central/database/files/000/dataset_1.dat using random seed 1"
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23 #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT NA00001 NA00002 NA00003
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24 20 1110696 rs6040355 A G,T 67 PASS AA=T;AF=0.333,0.667;DP=10;NS=2;DB GT:GQ:DP:HQ 1|2:21:6:23,27 2|1:2:0:18,2 2/2:35:4:.,.
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25 20 1230237 . T . 47 PASS AA=T;DP=13;NS=3 GT:GQ:DP:HQ 0|0:54:.:56,60 0|0:48:4:51,51 0/0:61:2:.,.
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26 X 10 rsTest AC A,ATG 10 PASS . GT 0 0/1 0|2
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