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. 2011 Aug 26;43(21):1207–1218. doi: 10.1152/physiolgenomics.00210.2010

Table 4.

Distribution of SHR sequence variants in c3-eQTL genes

Flanking Region
Transcript
Intronic
Gene Upstreama Downstreama 5′-UTRb Splice Sitec Silentd Nonsynonymouse 3′-UTRf Intron
Tst 30 19 0 0 2 0 0 30
Hp 32 2 0 0 0 0 0 1
Me3 3 30 0 0 1 0 0 142
Acox2 23 9 0 1 5 2 0 84
Ly6b 21 9 0 0 0 0 1 19
Cyp1a1 10 15 0 0 1 0 1 9
Akr1c1 8 15 0 0 0 1 3 37
Pex11b 8 10 0 2 0 2 2 27
Cela1 15 3 0 0 2 2 0 47
Trak2 7 3 1 1 1 0 1 111
Hpx 4 5 1 0 0 0 1 17
Cyp2d2 3 2 0 0 0 0 0 2
a

Region located within 5 kb upstream of the transcription initiation site or 5 kb downstream of transcript end.

b

Number of sequence variants in the 5′-untranslated region (UTR).

c

Number of sequence variants occurring in splice sites, i.e., the region located 1-3 bp into exon or 1-8 bp into an intron.

d

Number of sequence variants located in coding region that do not affect amino acid sequence.

e

Number of sequence variants located in coding region that do affect amino acid sequence.

f

Number of sequence variants in the 3′-UTR. c3-eQTL, colocalizing, correlated cis-eQTL.

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