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Table 1 Mapping of bovine candidate enhancers

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

dba

Queryb

Metf

m%g

Hitsh

eSNPl

ISeqc

u (bp)d

σ (bp)e

OSeqi

µ (bp)j

σ (bp)k

VISTA

4481

1959

1395

COM

4285 (96%)

9945

896

710

82,865

LO

3808 (85%)

964

1399

883

BN

3627 (81%)

9945

896

710

FANTOM5

109,882

277

158

COM

95,123 (87%)

30,371

231

115

50,447

LO

94,302 (86%)

6061

245

503

BN

10,054 (9%)

30,389

231

115

dbSUPER

1745

45,750

56,541

COM

1605 (92%)

50,938

739

763

282,285

LO

1549 (88%)

32

1916

2447

BN

1113 (64%)

50,938

739

763

H3K4me3

13,797

2393

879

NA

13,797 (100%)

13,660

2394

879

302,659

H3K27ac

45,784

2304

1910

NA

45,784 (100%)

42,963

2305

1910

965,716

  1. aDatabase from which input query sequences were obtained
  2. bQuery sequence downloaded from respective host sites (may include overlapping regions)
  3. cNumber of input enhancer query sequences
  4. dMean length of input enhancer query sequences (measured in bp)
  5. eStandard deviation length of input enhancer query sequences (measured in bp)
  6. fMethod that returned values in column m%; COM: a set of non-overlapping regions from the combined results of liftOver and BLASTn; LO: liftOver; BN: BLASTn
  7. gNumber of mapped query sequences (ratio of mapped query sequences); NA not applicable
  8. hHit is a non-overlapping genomic interval in the bovine genome that matches with at least one query sequence from the respective input database
  9. iNumber of non-overlapping candidate bovine enhancer genomic intervals; all hits, i.e. output from the respective software were merged into non-overlapping genomic intervals; some OSeq values were larger than corresponding ISeq values because one query sequence was found at multiple locations in the bovine genome
  10. jMean length of bovine putative enhancer sequences (measured in bp)
  11. kStandard deviation length of bovine putative enhancer sequences (measured in bp)
  12. lNumber of imputed whole-genome sequence variants in OSeq genomic intervals