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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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100794 SNVs 1 of 10080 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP002070912465 chr19: 26554 CR2 Intergenic T A
heterozygote
MACSNP002070912497 chr19: 28362 CR2 Intergenic G T
heterozygote
MACSNP002070912504 chr19: 28503 CR2 Intergenic G A
heterozygote
MACSNP002070912534 chr19: 29728 CR2 Intergenic G C
heterozygote
MACSNP002070912549 chr19: 30045 CR2 Intergenic A G
homozygote
MACSNP002070912555 chr19: 30139 CR2 Intergenic T C
homozygote
MACSNP002070912566 chr19: 30341 CR2 Intergenic A T
heterozygote
MACSNP002070912573 chr19: 30680 CR2 Intergenic C T
heterozygote
MACSNP002070912582 chr19: 30953 CR2 Intergenic C A
heterozygote
MACSNP002070912595 chr19: 33100 CR2 Intergenic T C
heterozygote

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