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Table 2 The information about the candidate SNPs in CYP3A4 and CYP11A1

From: CYP3A4 and CYP11A1 variants are risk factors for ischemic stroke: a case control study

Gene

SNP ID

Chr: Position

Alleles

(minor/major)

Frequency (MAF)

HaploReg

Case

Control

CYP3A4

rs3735451

7:99758352

C/T

0.26

0.30

Motifs Changed, Selected eQTL hits

CYP3A4

rs4646440

7:99763247

A/G

0.19

0.23

Promoter histone marks, Enhancer histone marks, DNAse, Proteins bound, Motifs changed, Selected eQTL hits

CYP3A4

rs35564277

7:99764813

C/T

0.06

0.07

Motifs Changed

CYP3A4

rs4646437

7:99767460

A/G

0.11

0.13

Promoter histone marks, Enhancer histone marks, Motifs changed, Selected eQTL hits

CYP11A1

rs1484215

15:74347768

T/C

0.18

0.18

Enhancer histone marks, Motifs changed, Selected eQTL hits

CYP11A1

rs12912592

15:74363369

T/G

0.10

0.08

Enhancer histone marks, Motifs changed, Selected eQTL hits

CYP11A1

rs28681535

15:74367268

T/G

0.43

0.45

Promoter histone marks, Enhancer histone marks, DNAse, Motifs changed

  1. MAF minor allele frequency, eQTL expression quantitative trait loci