Skip to main content

Table 3 Genome-wide significant loci by cross-trait meta-analysis at sentinel SNPs associated with COPD and HBP (Pmeta < 5 × 10− 8; single trait P < 0.01)

From: Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis

Sentinel SNP

CHR

N

Position

P HBP

P COPD

P META

Variant annotation

Genes within clumping region

rs12759054

1

72

chr1:234091759–234,196,884

1.2 × 10−6

5.78 × 10−3

4.88 × 10−8

Intron

SLC35F3

rs301819

1

99

chr1:8440643–8,895,970

1.3 × 10−10

5.47 × 10−3

9.93 × 10−12

Intron

RERE

rs305221

1

115

chr1:88899115–89,440,896

3.7 × 10−10

5.32 × 10−4

2.91 × 10−12

Intron

CCBL2, GTF2B, LOC101927891, PKN2

rs61781370

1

97

chr1:39554034–40,060,025

9.0 × 10−8

6.66 × 10−3

7.47 × 10−9

Upstream gene

BMP8A, KIAA0754, MACF1, PABPC4, PPIEL, SNORA55

rs71636784

1

198

chr1:26994245–27,298,564

3.60 × 10−10

0.002705

6.41 × 10−12

Intron

ARID1A, GPATCH3, GPN2, KDF1, NR0B2, NUDC, PIGV, SFN, ZDHHC18

rs2293947

3

153

chr3:127620467–128,349,376

1.0 × 10−8

1.96 × 10−3

9.09 × 10−10

Intron

C3orf27, DNAJB8, DNAJB8-AS1, EEFSEC, GATA2, KBTBD12, LOC90246, RPN1, RUVBL1, SEC61A1

rs6799272

3

163

chr3:157977793–158,421,824

2.0 × 10−8

2.55 × 10−3

1.22 × 10−9

Intron

GFM1, LOC100996447, LXN, MLF1, RARRES1, RSRC1

rs2869966

4

135

chr4:89750361–90,028,653

2.20 × 10−3

1.11 × 10−14

2.73 × 10−14

Intron

FAM13A

rs7655625

4

111

chr4:145228728–145,974,688

7.10 × 10−3

3.02 × 10−19

9.69 × 10−19

Intergenic

ANAPC10, HHIP, HHIP-AS1

rs7733088

5

66

chr5:147682118–147,856,522

1.50 × 10−3

4.41 × 10−14

1.26 × 10−13

Intron

FBXO38, HTR4, LOC102546294, SPINK7, SPINK9

rs9399401

6

15

chr6:142652344–142,865,106

4.20 × 10−3

3.59 × 10−10

9.38 × 10−10

Intron

GPR126, LOC153910

rs11771259

7

73

chr7:7174042–7,348,633

1.60 × 10−15

6.16 × 10−4

6.66 × 10−18

Intron

C1GALT1, LOC101927354

rs36044436

7

40

chr7:74027839–74,140,925

7.40 × 10−10

3.77 × 10−3

4.87 × 10−11

Intron

GTF2I, LOC101926943

rs633185

11

256

chr11:100421331–100,713,227

1.90 × 10−48

1.63 × 10− 4

1.80 × 10− 47

Intron

ARHGAP42

rs11168245

12

125

chr12:47981942–48,212,719

1.20 × 10−9

6.23 × 10−3

7.26 × 10−11

Intron

ENDOU, HDAC7, RAPGEF3, RPAP3, SLC48A1

rs1549306

16

95

chr16:75304623–75,491,327

4.0 × 10−9

7.61 × 10−4

3.36 × 10−11

Intron

CFDP1, TMEM170A

rs200528

16

58

chr16:24699511–24,879,963

1.70 × 10−7

1.86 × 10−3

1.37 × 10−8

Intron

SLC5A11, TNRC6A

rs4787486

16

26

chr16:29958216–30,093,779

1.10 × 10−8

8.61 × 10−3

7.10 × 10−9

Intron

ALDOA, C16orf92, DOC2A, FAM57B, HIRIP3, INO80E, PPP4C, TAOK2, TMEM219

rs55804009

18

72

chr18:1840658–1,902,417

9.0 × 10−9

7.36 × 10−3

6.62 × 10−10

Intergenic

LINC00470*

rs13040716

20

44

chr20:30660621–31,035,129

1.20 × 10−5

3.36 × 10−5

4.0 × 10−8

Downstream gene

ASXL1, HCK, KIF3B, NOL4L, PLAGL2, POFUT1, TM9SF4, TSPY26P

rs12627514

21

29

chr21:44740327–44,824,964

1.70 × 10−12

7.55 × 10−3

2.82 × 10−14

Intergenic

LINC00322

rs229340

21

173

chr21:44914815–45,133,868

6.10 × 10−11

9.87 × 10−3

1.57 × 10−11

Intron

HSF2BP, MIR6070, RRP1B

  1. SNP single nucleotide polymorphisms, CHR chromosome, HBP high blood pressure, COPD chronic obstructive pulmonary disease