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Table 2 SNVs in ROBO1 and 1-Mb upstream region on two samples from CGI and Illumina pooled samples

From: Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1

Genomic function Shared variantsa Shared heterozygotes Novel SNVsb
Exonic 0 0 0
Intronic 597 290 1
5′UTR 1 0 0
Upstream (1 Mb) 852 374 3
  1. aVariants showing in both Illumina pooled samples and two CGI individual samples
  2. bNot annotated in dbSNP version 137