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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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14259717 SNVs 1 of 1425972 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP015000000001 chr1: 9299 SM1 Intergenic G C
heterozygote
MACSNP016000000001 chr1: 9299 SM2 Intergenic G C
heterozygote
MACSNP003000000002 chr1: 9362 CR3 Intergenic C A
heterozygote
MACSNP004000000002 chr1: 9362 TW1 Intergenic C A
heterozygote
MACSNP020000000003 chr1: 9390 BM1 Intergenic G A
homozygote
MACSNP018000000004 chr1: 9415 PM2 Intergenic C T
heterozygote
MACSNP020000000005 chr1: 9428 BM1 Intergenic G T
homozygote
MACSNP020000000006 chr1: 9435 BM1 Intergenic C G
homozygote
MACSNP003000000007 chr1: 9492 CR3 Intergenic A G
heterozygote
MACSNP004000000007 chr1: 9492 TW1 Intergenic A G
heterozygote

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