Table 2 Independent association signals with a single CCV

From: Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes

Fine-mapping region

SNP

Chr

Position

Alleles

AF

OR (95% CI)

P valuea

Putative target gene(s)b

European-specific analysis

region_45

rs116000952

6

32541270

T/G

0.843

0.92 (0.89–0.96)

5.74E−06

region_45

rs6920820

6

30969938

C/G

0.980

0.84 (0.79–0.90)

6.87E−08

LINC00243

region_61

rs72681666

8

117641754

T/C

0.043

1.09 (1.05–1.13)

1.57E−05

region_62

rs77569096

8

128468955

A/G

0.763

0.92 (0.90–0.94)

2.06E−15

region_84

rs3217810

12

4388271

T/C

0.127

1.13 (1.11–1.16)

1.96E−26

region_108

rs144674978

15

33149751

T/C

0.013

1.34 (1.25–1.43)

1.11E−18

region_133

rs149942633

20

48983073

T/C

0.153

1.12 (1.08–1.16)

1.93E−08

Trans-ancestry analysis

region_1

rs112191583

1

22554378

T/C

0.974

0.88 (0.83–0.92)

1.19E−07

region_24

rs704417

3

64252424

T/C

0.546

1.05 (1.03–1.06)

4.35E−10

region_27

rs113569514

3

133748789

T/C

0.763

1.08 (1.07–1.10)

1.92E−21

SLCO2A1

region_29

rs2578155

4

94836291

C/G

0.503

1.04 (1.03–1.06)

1.09E−09

region_42

rs9379084

6

7231843

A/G

0.144

0.93 (0.91–0.95)

2.39E−12

RREB1

region_46

rs16878812

6

35569562

A/G

0.892

1.09 (1.07–1.12)

7.62E−15

FKBP5

region_48

rs6933790

6

41672769

T/C

0.788

1.08 (1.06–1.10)

2.66E−20

region_61

rs4129064

8

117735666

T/G

0.734

1.06 (1.04–1.07)

1.01E−09

region_62

rs6983267

8

128413305

T/G

0.508

0.86 (0.85–0.87)

1.65E−122

MYC

region_72

rs704017

10

80819132

A/G

0.473

0.92 (0.91–0.93)

1.97E−38

region_84

rs12818766

12

4376091

A/G

0.215

1.10 (1.08–1.12)

1.81E−29

region_89

rs7398375

12

57540848

C/G

0.651

1.07 (1.05–1.09)

3.70E−19

LRP1

region_94

rs11067228

12

115094260

A/G

0.560

0.95 (0.94–0.97)

2.50E−13

region_96

rs116964464

13

27543193

T/C

0.035

1.11 (1.07–1.15)

4.83E−09

USP12

region_99

rs7325844

13

73625133

A/G

0.639

1.05 (1.04–1.07)

1.28E−12

region_104

rs35107139

14

54419106

A/C

0.550

0.92 (0.91–0.93)

4.22E−36

region_105

rs8020436

14

59208437

A/G

0.370

1.06 (1.05–1.08)

1.27E−17

region_108

rs17816465

15

33156386

A/G

0.193

1.09 (1.07–1.10)

5.73E−20

region_116

rs1078643

17

10707241

A/G

0.765

1.09 (1.07–1.11)

2.31E−27

region_132

rs6066825

20

47340117

A/G

0.662

1.08 (1.07–1.10)

2.13E−32

region_136

rs1741640

20

60932414

T/C

0.208

0.88 (0.86–0.89)

8.15E−55

LAMA5, CABLES2

  1. Chr and Position GRCh37, Alleles risk allele/Reference allele, AF Allele frequency, OR odds ratio, CI confidence interval. aP value derived from trans-ancestry or European-ancestry meta-analysis under the fixed-effects inverse variance weighted model; b”-“ – No target genes were prioritized for the variant in this study.