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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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688127 SNVs 1 of 68813 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014031370885 chr7: 18881 AM1 Intergenic A T
heterozygote
MACSNP014031370889 chr7: 18929 AM1 Intergenic C T
heterozygote
MACSNP014031370891 chr7: 18947 AM1 Intergenic C G
heterozygote
MACSNP014031370989 chr7: 29282 AM1 Intergenic G T
homozygote
MACSNP014031370990 chr7: 29328 AM1 Intergenic G A
heterozygote
MACSNP014031370992 chr7: 29412 AM1 Intergenic C T
homozygote
MACSNP014031371004 chr7: 29815 AM1 Intergenic C T
homozygote
MACSNP014031371055 chr7: 33710 AM1 Intergenic C T
heterozygote
MACSNP014031371057 chr7: 33749 AM1 Intergenic A G
heterozygote
MACSNP014031371059 chr7: 33791 AM1 Intergenic A T
heterozygote

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