##fichierformat=VCFv4.2 
##fichierDate=20220220
##source=myImputationProgramV3.1
##reference=NM_016124.6
##contig=<ID= chr1 ,length=2814,species='Homo sapiens',taxonomy=9606>
##phasing=partial
##INFO=<ID=NS,Number=1,Type=Integer,Description='Number of Samples With Data'>
##INFO=<ID=DP,Number=1,Type=Integer,Description='Total Depth'>
##INFO=<ID=AF,Number=A,Type=Float,Description='Allele Frequency'>
##INFO=<ID=AA,Number=1,Type=String,Description='Ancestral Allele'>##INFO=<ID=DB,Number=0,Type=Flag,Description='dbSNP membership, build 129'>
##INFO=<ID=H2,Number=0,Type=Flag,Description='HapMap2 membership'>
##FILTER=<ID=q10,Description='Quality below 10'>
##FILTER=<ID=s50,Description='Less than 50 of samples have data'>
##FORMAT=<ID=GT,Number=1,Type=String,Description='Genotype'>
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
##FORMAT=<ID=HQ,Number=2,Type=Integer,Description="Haplotype Quality">
#CHROM   POS         ID  REF  ALT QUAL FILTER    INFO
   chr1   916  RHef00069    G    A    .   PASS  DP=100
   chr1   932  RHef00069    A    G    .   PASS  DP=100
   chr1   941  RHef00069    G    T    .   PASS  DP=100
   chr1   968  RHef00069    C    A    .   PASS  DP=100
   chr1   974  RHef00069    G    T    .   PASS  DP=100
   chr1   979  RHef00069    A    G    .   PASS  DP=100
   chr1   985  RHef00069   GG   CA    .   PASS  DP=100
   chr1   989  RHef00069    A    C    .   PASS  DP=100
   chr1   992  RHef00069    A    T    .   PASS  DP=100
   chr1  1025  RHef00069    T    C    .   PASS  DP=100
   chr1  1048  RHef00069    G    C    .   PASS  DP=100
   chr1  1053  RHef00069    C    T    .   PASS  DP=100
   chr1  1057  RHef00069  GGA  TGG    .   PASS  DP=100
   chr1  1060  RHef00069   GC   AA    .   PASS  DP=100
   chr1  1170  RHef00069    T    C    .   PASS  DP=100
   chr1  1193  RHef00069    A    T    .   PASS  DP=100