view test-data/update_genomes_test_data/W1118_snp_testGenes.vcf @ 0:e979cb57a5d5 draft default tip

"planemo upload for repository https://github.com/McIntyre-Lab/BayesASE/tree/main/galaxy commit 9b70598ef46a73632d9e0fa0c6ce6776fb5e9d6a"
author malex
date Thu, 14 Jan 2021 21:51:36 +0000
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##fileformat=VCFv4.2
##ALT=<ID=NON_REF,Description="Represents any possible alternative allele at this location">
##FILTER=<ID=Het,Description="isHet == 1">
##FILTER=<ID=LowQual,Description="Low quality">
##FILTER=<ID=PASS,Description="All filters passed">
##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth (reads with MQ=255 or with bad mates are filtered)">
##FORMAT=<ID=FT,Number=.,Type=String,Description="Genotype-level filter">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=MIN_DP,Number=1,Type=Integer,Description="Minimum DP observed within the GVCF block">
##FORMAT=<ID=PL,Number=G,Type=Integer,Description="Normalized, Phred-scaled likelihoods for genotypes as defined in the VCF specification">
##FORMAT=<ID=SB,Number=4,Type=Integer,Description="Per-sample component statistics which comprise the Fisher's Exact Test to detect strand bias.">
##GATKCommandLine=<ID=GenotypeGVCFs,Version=3.2-2-gec30cee,Date="Fri Aug 22 11:38:29 PDT 2014",Epoch=1408732709322,CommandLineOptions="analysis_type=GenotypeGVCFs input_file=[] showFullBamList=false read_buffer_size=null phone_home=AWS gatk_key=null tag=NA read_filter=[] intervals=null excludeIntervals=null interval_set_rule=UNION interval_merging=ALL interval_padding=0 reference_sequence=/home/rcf-40/msalomon/cmb/CEGS_fly_sequencing/reference/dmel-all-chromosome-r5.41_edited_headers.fasta nonDeterministicRandomSeed=false disableDithering=false maxRuntime=-1 maxRuntimeUnits=MINUTES downsampling_type=BY_SAMPLE downsample_to_fraction=null downsample_to_coverage=1000 baq=OFF baqGapOpenPenalty=40.0 refactor_NDN_cigar_string=false fix_misencoded_quality_scores=false allow_potentially_misencoded_quality_scores=false useOriginalQualities=false defaultBaseQualities=-1 performanceLog=null BQSR=null quantize_quals=0 disable_indel_quals=false emit_original_quals=false preserve_qscores_less_than=6 globalQScorePrior=-1.0 validation_strictness=SILENT remove_program_records=false keep_program_records=false sample_rename_mapping_file=null unsafe=null disable_auto_index_creation_and_locking_when_reading_rods=false num_threads=1 num_cpu_threads_per_data_thread=1 num_io_threads=0 monitorThreadEfficiency=false num_bam_file_handles=null read_group_black_list=null pedigree=[] pedigreeString=[] pedigreeValidationType=STRICT allow_intervals_with_unindexed_bam=false generateShadowBCF=false variant_index_type=DYNAMIC_SEEK variant_index_parameter=-1 logging_level=INFO log_to_file=null help=false version=false variant=[(RodBindingCollection [(RodBinding name=variant source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/DGRP_48.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant2 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/DGRP_382.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant3 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source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_68.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant227 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_69.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant228 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_70.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant229 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_74.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant230 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_76.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant231 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_79.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant232 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_80.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant233 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_82.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant234 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_84.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant235 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_86.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant236 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_87.raw.SNPs.and.indels.g.vcf)]), (RodBindingCollection [(RodBinding name=variant237 source=/home/cmb-07/sn1/msalomon/CEGS_HaplotypeCaller/g_vcfs/Winters_114.raw.SNPs.and.indels.g.vcf)])] out=org.broadinstitute.gatk.engine.io.stubs.VariantContextWriterStub no_cmdline_in_header=org.broadinstitute.gatk.engine.io.stubs.VariantContextWriterStub sites_only=org.broadinstitute.gatk.engine.io.stubs.VariantContextWriterStub bcf=org.broadinstitute.gatk.engine.io.stubs.VariantContextWriterStub includeNonVariantSites=false annotateNDA=false heterozygosity=0.001 indel_heterozygosity=1.25E-4 standard_min_confidence_threshold_for_calling=30.0 standard_min_confidence_threshold_for_emitting=30.0 max_alternate_alleles=6 input_prior=[] sample_ploidy=2 annotation=[InbreedingCoeff, FisherStrand, QualByDepth, ChromosomeCounts, GenotypeSummaries] dbsnp=(RodBinding name= source=UNBOUND) filter_reads_with_N_cigar=false filter_mismatching_base_and_quals=false filter_bases_not_stored=false">
##GATKCommandLine=<ID=SelectVariants,CommandLine="SelectVariants  --output /ufrc/mcintyre/share/BASE_mclab/galaxy/vcf_by_genotype/W1118_snp.vcf --sample-name W1118 --exclude-non-variants true --variant /ufrc/mcintyre/share/mel_cegs_variant_info/vcf_files_v3/CEGS.237.lines.SNPs.filtered.set.1.recode.vcf --reference /ufrc/mcintyre/share/references/dmel_fb551/dmel-all-chromosome-r5.51.fasta  --invertSelect false --exclude-filtered false --preserve-alleles false --remove-unused-alternates false --restrict-alleles-to ALL --keep-original-ac false --keep-original-dp false --mendelian-violation false --invert-mendelian-violation false --mendelian-violation-qual-threshold 0.0 --select-random-fraction 0.0 --remove-fraction-genotypes 0.0 --fully-decode false --max-indel-size 2147483647 --min-indel-size 0 --max-filtered-genotypes 2147483647 --min-filtered-genotypes 0 --max-fraction-filtered-genotypes 1.0 --min-fraction-filtered-genotypes 0.0 --max-nocall-number 2147483647 --max-nocall-fraction 1.0 --set-filtered-gt-to-nocall false --allow-nonoverlapping-command-line-samples false --suppress-reference-path false --interval-set-rule UNION --interval-padding 0 --interval-exclusion-padding 0 --interval-merging-rule ALL --read-validation-stringency SILENT --seconds-between-progress-updates 10.0 --disable-sequence-dictionary-validation false --create-output-bam-index true --create-output-bam-md5 false --create-output-variant-index true --create-output-variant-md5 false --lenient false --add-output-sam-program-record true --add-output-vcf-command-line true --cloud-prefetch-buffer 40 --cloud-index-prefetch-buffer -1 --disable-bam-index-caching false --sites-only-vcf-output false --help false --version false --showHidden false --verbosity INFO --QUIET false --use-jdk-deflater false --use-jdk-inflater false --gcs-max-retries 20 --gcs-project-for-requester-pays  --disable-tool-default-read-filters false",Version="4.1.4.0",Date="July 22, 2020 1:43:15 PM EDT">
##GVCFBlock=minGQ=0(inclusive),maxGQ=5(exclusive)
##INFO=<ID=AC,Number=A,Type=Integer,Description="Allele count in genotypes, for each ALT allele, in the same order as listed">
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency, for each ALT allele, in the same order as listed">
##INFO=<ID=AN,Number=1,Type=Integer,Description="Total number of alleles in called genotypes">
##INFO=<ID=BaseQRankSum,Number=1,Type=Float,Description="Z-score from Wilcoxon rank sum test of Alt Vs. Ref base qualities">
##INFO=<ID=CCC,Number=1,Type=Integer,Description="Number of called chromosomes">
##INFO=<ID=ClippingRankSum,Number=1,Type=Float,Description="Z-score From Wilcoxon rank sum test of Alt vs. Ref number of hard clipped bases">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth; some reads may have been filtered">
##INFO=<ID=DS,Number=0,Type=Flag,Description="Were any of the samples downsampled?">
##INFO=<ID=END,Number=1,Type=Integer,Description="Stop position of the interval">
##INFO=<ID=FS,Number=1,Type=Float,Description="Phred-scaled p-value using Fisher's exact test to detect strand bias">
##INFO=<ID=GQ_MEAN,Number=1,Type=Float,Description="Mean of all GQ values">
##INFO=<ID=GQ_STDDEV,Number=1,Type=Float,Description="Standard deviation of all GQ values">
##INFO=<ID=HWP,Number=1,Type=Float,Description="P value from test of Hardy Weinberg Equilibrium">
##INFO=<ID=HaplotypeScore,Number=1,Type=Float,Description="Consistency of the site with at most two segregating haplotypes">
##INFO=<ID=InbreedingCoeff,Number=1,Type=Float,Description="Inbreeding coefficient as estimated from the genotype likelihoods per-sample when compared against the Hardy-Weinberg expectation">
##INFO=<ID=MLEAC,Number=A,Type=Integer,Description="Maximum likelihood expectation (MLE) for the allele counts (not necessarily the same as the AC), for each ALT allele, in the same order as listed">
##INFO=<ID=MLEAF,Number=A,Type=Float,Description="Maximum likelihood expectation (MLE) for the allele frequency (not necessarily the same as the AF), for each ALT allele, in the same order as listed">
##INFO=<ID=MQ,Number=1,Type=Float,Description="RMS Mapping Quality">
##INFO=<ID=MQ0,Number=1,Type=Integer,Description="Total Mapping Quality Zero Reads">
##INFO=<ID=MQRankSum,Number=1,Type=Float,Description="Z-score From Wilcoxon rank sum test of Alt vs. Ref read mapping qualities">
##INFO=<ID=NCC,Number=1,Type=Integer,Description="Number of no-called samples">
##INFO=<ID=QD,Number=1,Type=Float,Description="Variant Confidence/Quality by Depth">
##INFO=<ID=ReadPosRankSum,Number=1,Type=Float,Description="Z-score from Wilcoxon rank sum test of Alt vs. Ref read position bias">
##SelectVariants="analysis_type=SelectVariants input_file=[] read_buffer_size=null phone_home=STANDARD gatk_key=null tag=NA read_filter=[] intervals=null excludeIntervals=null interval_set_rule=UNION interval_merging=ALL interval_padding=0 reference_sequence=/Users/msalomon/Desktop/reference/dmel-all-chromosome-r5.41_edited_headers.fasta nonDeterministicRandomSeed=false disableDithering=false maxRuntime=-1 maxRuntimeUnits=MINUTES downsampling_type=BY_SAMPLE downsample_to_fraction=null downsample_to_coverage=1000 baq=OFF baqGapOpenPenalty=40.0 fix_misencoded_quality_scores=false allow_potentially_misencoded_quality_scores=false performanceLog=null useOriginalQualities=false BQSR=null quantize_quals=0 disable_indel_quals=false emit_original_quals=false preserve_qscores_less_than=6 globalQScorePrior=-1.0 allow_bqsr_on_reduced_bams_despite_repeated_warnings=false defaultBaseQualities=-1 validation_strictness=SILENT remove_program_records=false keep_program_records=false unsafe=null disable_auto_index_creation_and_locking_when_reading_rods=false num_threads=8 num_cpu_threads_per_data_thread=1 num_io_threads=0 monitorThreadEfficiency=false num_bam_file_handles=null read_group_black_list=null pedigree=[] pedigreeString=[] pedigreeValidationType=STRICT allow_intervals_with_unindexed_bam=false generateShadowBCF=false logging_level=INFO log_to_file=null help=false version=false variant=(RodBinding name=variant source=CEGS.ALL.snp.and.indel.raw.HETS.marked.vcf) discordance=(RodBinding name= source=UNBOUND) concordance=(RodBinding name= source=UNBOUND) out=org.broadinstitute.sting.gatk.io.stubs.VariantContextWriterStub no_cmdline_in_header=org.broadinstitute.sting.gatk.io.stubs.VariantContextWriterStub sites_only=org.broadinstitute.sting.gatk.io.stubs.VariantContextWriterStub bcf=org.broadinstitute.sting.gatk.io.stubs.VariantContextWriterStub sample_name=[] sample_expressions=null sample_file=null exclude_sample_name=[] exclude_sample_file=[] select_expressions=[] excludeNonVariants=true excludeFiltered=false restrictAllelesTo=ALL keepOriginalAC=false mendelianViolation=false mendelianViolationQualThreshold=0.0 select_random_fraction=0.0 remove_fraction_genotypes=0.0 selectTypeToInclude=[SNP] keepIDs=null fullyDecode=false forceGenotypesDecode=false justRead=false maxIndelSize=2147483647 ALLOW_NONOVERLAPPING_COMMAND_LINE_SAMPLES=false filter_mismatching_base_and_quals=false filter_bases_not_stored=false"
##VariantFiltration="analysis_type=VariantFiltration input_file=[] read_buffer_size=null phone_home=STANDARD gatk_key=null tag=NA read_filter=[] intervals=null excludeIntervals=null interval_set_rule=UNION interval_merging=ALL interval_padding=0 reference_sequence=/Users/msalomon/Desktop/reference/dmel-all-chromosome-r5.41_edited_headers.fasta nonDeterministicRandomSeed=false disableDithering=false maxRuntime=-1 maxRuntimeUnits=MINUTES downsampling_type=BY_SAMPLE downsample_to_fraction=null downsample_to_coverage=1000 baq=OFF baqGapOpenPenalty=40.0 fix_misencoded_quality_scores=false allow_potentially_misencoded_quality_scores=false performanceLog=null useOriginalQualities=false BQSR=null quantize_quals=0 disable_indel_quals=false emit_original_quals=false preserve_qscores_less_than=6 globalQScorePrior=-1.0 allow_bqsr_on_reduced_bams_despite_repeated_warnings=false defaultBaseQualities=-1 validation_strictness=SILENT remove_program_records=false keep_program_records=false unsafe=null disable_auto_index_creation_and_locking_when_reading_rods=false num_threads=1 num_cpu_threads_per_data_thread=1 num_io_threads=0 monitorThreadEfficiency=false num_bam_file_handles=null read_group_black_list=null pedigree=[] pedigreeString=[] pedigreeValidationType=STRICT allow_intervals_with_unindexed_bam=false generateShadowBCF=false logging_level=INFO log_to_file=null help=false version=false variant=(RodBinding name=variant source=CEGS.ALL.snp.and.indel.raw.vcf) mask=(RodBinding name= source=UNBOUND) out=org.broadinstitute.sting.gatk.io.stubs.VariantContextWriterStub no_cmdline_in_header=org.broadinstitute.sting.gatk.io.stubs.VariantContextWriterStub sites_only=org.broadinstitute.sting.gatk.io.stubs.VariantContextWriterStub bcf=org.broadinstitute.sting.gatk.io.stubs.VariantContextWriterStub filterExpression=[] filterName=[] genotypeFilterExpression=[isHet == 1] genotypeFilterName=[Het] clusterSize=3 clusterWindowSize=0 maskExtension=0 maskName=Mask filterNotInMask=false missingValuesInExpressionsShouldEvaluateAsFailing=false invalidatePreviousFilters=false filter_mismatching_base_and_quals=false filter_bases_not_stored=false"
##bcftools_viewCommand=view -O v -o /ufrc/mcintyre/share/mel_cegs_variant_info/vcf_files_v3/CEGS.237.lines.SNPs.filtered.set.1.recode.vcf /ufrc/mcintyre/share/mel_cegs_variant_info/vcf_files_v3/CEGS.237.lines.SNPs.filtered.set.1.recode.vcf.gz; Date=Wed Jul 22 13:40:32 2020
##bcftools_viewVersion=1.10.2+htslib-1.10.2
##contig=<ID=YHet,length=347038,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=dmel_mitochondrion_genome,length=19517,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=2L,length=23011544,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=X,length=22422827,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=3L,length=24543557,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=4,length=1351857,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=2R,length=21146708,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=3R,length=27905053,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=Uextra,length=29004656,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=2RHet,length=3288761,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=2LHet,length=368872,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=3LHet,length=2555491,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=3RHet,length=2517507,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=U,length=10049037,assembly=dmel-all-chromosome-r5.51.fasta>
##contig=<ID=XHet,length=204112,assembly=dmel-all-chromosome-r5.51.fasta>
##reference=file:///ufrc/mcintyre/share/references/dmel_fb551/dmel-all-chromosome-r5.51.fasta
##source=SelectVariants
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	W1118
X	7781305	.	G	C	17318.70	PASS	AC=2;AF=1.00;AN=2;DP=9	GT:AD:DP:GQ:PL	1/1:0,9:9:30:432,30,0
X	21889635	.	C	T	30606.60	PASS	AC=2;AF=1.00;AN=2;DP=6	GT:AD:DP:GQ:PL	1/1:0,6:6:18:230,18,0
X	21889661	.	G	C	70712.10	PASS	AC=2;AF=1.00;AN=2;DP=8	GT:AD:DP:GQ:PL	1/1:0,8:8:24:286,24,0
X	21889690	.	A	C	22562.60	PASS	AC=2;AF=1.00;AN=2;DP=6	GT:AD:DP:GQ:PL	1/1:0,6:6:18:270,18,0
X	21889694	.	G	A	68972.30	PASS	AC=2;AF=1.00;AN=2;DP=6	GT:AD:DP:GQ:PL	1/1:0,6:6:18:270,18,0
X	21890117	.	A	T	53529.60	PASS	AC=2;AF=1.00;AN=2;DP=12	GT:AD:DP:GQ:PL	1/1:0,12:12:36:472,36,0
X	21893636	.	C	T	76735.40	PASS	AC=2;AF=1.00;AN=2;DP=12	GT:AD:DP:GQ:PL	1/1:0,9:12:36:0,12,0
X	21893803	.	C	T	58173.10	PASS	AC=2;AF=1.00;AN=2;DP=5	GT:AD:DP:GQ:PL	1/1:0,5:5:15:208,15,0
X	21894302	.	T	A	71351.10	PASS	AC=2;AF=1.00;AN=2;DP=14	GT:AD:DP:GQ:PL	1/1:0,14:14:42:593,42,0
X	21895115	.	T	C	66417.80	PASS	AC=2;AF=1.00;AN=2;DP=13	GT:AD:DP:GQ:PL	1/1:0,13:13:39:564,39,0
X	21895236	.	T	A	84196.40	PASS	AC=2;AF=1.00;AN=2;DP=19	GT:AD:DP:GQ:PL	1/1:0,19:19:57:787,57,0
X	21895556	.	A	G	107863	PASS	AC=2;AF=1.00;AN=2;DP=11	GT:AD:DP:GQ:PL	1/1:0,11:11:33:478,33,0
X	21895559	.	G	A	52330.70	PASS	AC=2;AF=1.00;AN=2;DP=9	GT:AD:DP:GQ:PL	1/1:0,9:9:30:444,30,0
X	21895697	.	T	C	110094	PASS	AC=2;AF=1.00;AN=2;DP=17	GT:AD:DP:GQ:PL	1/1:0,17:17:51:690,51,0
X	21896185	.	C	A	5071.21	PASS	AC=2;AF=1.00;AN=2;DP=17	GT:AD:DP:GQ:PL	1/1:0,17:17:51:720,51,0
X	21897092	.	G	T	14573.70	PASS	AC=2;AF=1.00;AN=2;DP=15	GT:AD:DP:GQ:PL	1/1:0,15:15:45:650,45,0
X	21898037	.	T	G	99430.60	PASS	AC=2;AF=1.00;AN=2;DP=8	GT:AD:DP:GQ:PL	1/1:0,8:8:30:440,30,0
X	21898046	.	T	G	88654.70	PASS	AC=2;AF=1.00;AN=2;DP=13	GT:AD:DP:GQ:PL	1/1:0,13:13:39:544,39,0
X	21898238	.	C	T	51144.70	PASS	AC=2;AF=1.00;AN=2;DP=13	GT:AD:DP:GQ:PL	1/1:0,13:13:39:519,39,0
X	21898641	.	T	C	66103.40	PASS	AC=2;AF=1.00;AN=2;DP=14	GT:AD:DP:GQ:PL	1/1:0,14:14:42:569,42,0
X	21899027	.	T	G	42283.40	PASS	AC=2;AF=1.00;AN=2;DP=11	GT:AD:DP:GQ:PL	1/1:0,11:11:33:420,33,0
X	21899043	.	T	A	61169.20	PASS	AC=2;AF=1.00;AN=2;DP=8	GT:AD:DP:GQ:PL	1/1:0,8:8:24:337,24,0
X	21899576	.	C	T	83305.10	PASS	AC=2;AF=1.00;AN=2;DP=12	GT:AD:DP:GQ:PL	1/1:0,12:12:36:473,36,0
X	21899675	.	T	C	139002	PASS	AC=2;AF=1.00;AN=2;DP=17	GT:AD:DP:GQ:PL	1/1:0,17:17:51:708,51,0
X	21899720	.	C	T	10772.70	PASS	AC=2;AF=1.00;AN=2;DP=20	GT:AD:DP:GQ:PL	1/1:0,20:20:60:862,60,0
X	21899903	.	T	C	12674	PASS	AC=2;AF=1.00;AN=2;DP=18	GT:AD:DP:GQ:PL	1/1:0,18:18:54:768,54,0
X	21900307	.	A	G	80133.80	PASS	AC=2;AF=1.00;AN=2;DP=11	GT:AD:DP:GQ:PL	1/1:0,11:11:33:472,33,0
X	21900768	.	G	T	74693.30	PASS	AC=2;AF=1.00;AN=2;DP=14	GT:AD:DP:GQ:PL	1/1:0,14:14:42:592,42,0
X	21900780	.	A	G	65714.90	PASS	AC=2;AF=1.00;AN=2;DP=14	GT:AD:DP:GQ:PL	1/1:0,14:14:42:571,42,0
X	21901775	.	T	C	22131.50	PASS	AC=2;AF=1.00;AN=2;DP=10	GT:AD:DP:GQ:PL	1/1:0,10:10:30:429,30,0
X	21902059	.	C	T	10715.30	PASS	AC=2;AF=1.00;AN=2;DP=11	GT:AD:DP:GQ:PL	1/1:0,11:11:33:453,33,0
X	21902804	.	C	T	75910.80	PASS	AC=2;AF=1.00;AN=2;DP=6	GT:AD:DP:GQ:PL	1/1:0,6:6:18:251,18,0
X	21902864	.	G	A	62085.10	PASS	AC=2;AF=1.00;AN=2;DP=10	GT:AD:DP:GQ:PL	1/1:0,10:10:30:450,30,0
X	21902872	.	T	A	83073.30	PASS	AC=2;AF=1.00;AN=2;DP=13	GT:AD:DP:GQ:PL	1/1:0,13:13:39:529,39,0
X	21903096	.	G	A	40162.90	PASS	AC=2;AF=1.00;AN=2;DP=13	GT:AD:DP:GQ:PL	1/1:0,13:13:39:515,39,0
X	21903162	.	T	C	52615.90	PASS	AC=2;AF=1.00;AN=2;DP=16	GT:AD:DP:GQ:PL	1/1:0,16:16:48:622,48,0
X	21903300	.	A	C	52197.30	PASS	AC=2;AF=1.00;AN=2;DP=13	GT:AD:DP:GQ:PL	1/1:0,13:13:39:502,0,0
X	21903317	.	C	A	39534.20	PASS	AC=2;AF=1.00;AN=2;DP=15	GT:AD:DP:GQ:PL	1/1:0,15:15:45:577,45,0
X	21903354	.	T	G	53570.10	PASS	AC=2;AF=1.00;AN=2;DP=13	GT:AD:DP:GQ:PL	1/1:0,13:13:39:504,39,0
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