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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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772903 SNVs 1 of 77291 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP014026079065 chr6: 17502 AM1 Intergenic C T
homozygote
MACSNP014026079090 chr6: 25025 AM1 Intergenic G C
homozygote
MACSNP014026079092 chr6: 25122 AM1 Intergenic C G
heterozygote
MACSNP014026079101 chr6: 27316 AM1 Intergenic G A
heterozygote
MACSNP014026079107 chr6: 28178 AM1 Intergenic C T
homozygote
MACSNP014026079112 chr6: 28939 AM1 Intergenic G T
homozygote
MACSNP014026079114 chr6: 28980 AM1 Intergenic A T
homozygote
MACSNP014026079127 chr6: 38929 AM1 Intergenic C T
homozygote
MACSNP014026079129 chr6: 38968 AM1 Intergenic G A
homozygote
MACSNP014026079130 chr6: 39077 AM1 Intergenic T C
homozygote

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