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Filter SNVs Using Feature Selection

Chromosome chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20
Individual All CR1 CR2 CR3 TW1 JM1 JM2 CE1 CE2 CE3 CE4 CE5 TM1 TM2 AM1 SM1 SM2 PM1 PM2 LM1 BM1
Gene feature All CDS EXON 3'UTR INTRON 5'UTR Genotype All homozygote heterozygote Mutation All non-synonymous synonymous
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342142 SNVs 1 of 34215 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002031370822 chr7: 5433 CR2 Intergenic C T
heterozygote
MACSNP002031370848 chr7: 10577 CR2 Intergenic A G
homozygote
MACSNP002031370851 chr7: 10682 CR2 Intergenic A G
heterozygote
MACSNP002031370887 chr7: 18897 CR2 Intergenic C T
heterozygote
MACSNP002031370889 chr7: 18929 CR2 Intergenic C T
heterozygote
MACSNP002031370982 chr7: 29074 CR2 Intergenic G C
heterozygote
MACSNP002031371016 chr7: 30777 CR2 Intergenic G A
heterozygote
MACSNP002031371017 chr7: 30804 CR2 Intergenic G A
heterozygote
MACSNP002031371026 chr7: 31594 CR2 Intergenic A G
heterozygote
MACSNP002031371028 chr7: 31632 CR2 Intergenic T C
heterozygote

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