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Table 5 Enrichment of significant enhancer SNPs \(\left( {P \le 10^{ - 8} } \right)\) for milk production traits in the permutation tests

From: Putative enhancer sites in the bovine genome are enriched with variants affecting complex traits

Phenotype

Database

All SNPs/a subset of SNPs

Fold changea

Rankb

FY

VISTA

All

0.16235

0.0001

MY

0.336793

0.0001

PY

0

0.0001

FY

FANTOM5

0.200888

0.0001

MY

0.414773

0.0018

PY

0.096781

0.0001

FY

dbSUPER

0.226716

0.0001

MY

0.354855

0.0001

PY

0.329258

0.0001

FY

Villar (H3K4me3)

2.892337

<0.0001

MY

2.100798

<0.0001

PY

3.081699

<0.0001

FY

Villar (H3K27ac)

1.459357

<0.0001

MY

1.29579

<0.0001

PY

1.458739

<0.0001

FY

Villar:H3K4me3

H3K4me3-specific only

3.358042

<0.0001

MY

 

2.440737

<0.0001

PY

 

4.414017

<0.0001

FY

Villar:H3K27ac

H3K27ac-sepcific only

0.967677

0.3063

MY

 

1.023431

0.647

PY

 

0.953471

0.2794

FY

Villar:H3K4me3 and H3K27ac

Overlaps: H3K4me3 and H3K27ac

2.795722

<0.0001

MY

 

2.025759

<0.0001

PY

 

2.801491

<0.0001

  1. aFold change is the ratio between the actual number of significant SNPs in an enhancer set and the mean number of all significant SNPs in the 10,000 random samples
  2. bRanking position of the actual number of significant SNPs in an enhancer set within the distribution of all the numbers of significant SNPs for the 10,000 random samples; if the actual number of significant SNPs was the largest among all the numbers of the 10,000 random significant SNPs, the rank was set to <0.0001; otherwise it was denoted as the ranking position of the actual number of significant SNPs among the number of random significant SNPs