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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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493597 SNVs 1 of 49360 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP006026079083 chr6: 24210 JM2 Intergenic A G
heterozygote
MACSNP006026079084 chr6: 24358 JM2 Intergenic G A
heterozygote
MACSNP006026079097 chr6: 25941 JM2 Intergenic G A
heterozygote
MACSNP006026079104 chr6: 27489 JM2 Intergenic T G
homozygote
MACSNP006026079107 chr6: 28178 JM2 Intergenic C T
homozygote
MACSNP006026079109 chr6: 28558 JM2 Intergenic C T
heterozygote
MACSNP006026079120 chr6: 31233 JM2 Intergenic T G
homozygote
MACSNP006026079128 chr6: 38943 JM2 Intergenic T C
heterozygote
MACSNP006026079138 chr6: 39787 JM2 Intergenic C A
homozygote
MACSNP006026079139 chr6: 39912 JM2 Intergenic C A
heterozygote

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