Skip to main content

Table 2 Functions and diseases related to both CEU and YRI signatures

From: Fine-scale detection of population-specific linkage disequilibrium using haplotype entropy in the human genome

 

CEU

YRI

Diabetes

1.70E-17

2.70E-20

Coronary artery disease

3.78E-17

3.12E-13

Genetic disorder

1.09E-14

4.53E-14

Cardiovascular disease

1.34E-14

4.78E-11

Non-insulin-dependent diabetes mellitus

1.03E-12

8.66E-15

Endocrine system disorder

1.91E-12

1.25E-18

Hypertension

2.13E-12

2.83E-11

Neurological disorder

2.49E-12

3.27E-12

Crohn's disease

7.59E-12

7.25E-09

Bipolar affective disease

3.50E-11

5.24E-09

Metabolic disorder

5.66E-11

9.83E-16

Inflammatory disorder

2.56E-09

1.08E-08

Digestive system disorder

2.66E-09

1.31E-07

Skeletal and muscular disorder

1.49E-08

1.58E-08

Progressive motor neuropathy

2.53E-08

5.59E-12

Autoimmune disease

7.28E-08

1.09E-12

Immunological disorder

2.46E-07

3.66E-13

Rheumatoid arthritis

3.78E-07

2.54E-07

Shape change of epithelial cells

8.86E-07

 

Alzheimer's disease

3.60E-06

2.27E-07

Parkinson's disease

7.24E-06

5.29E-06

Shape change of dermal cells

9.33E-06

 

Insulin-dependent diabetes mellitus

 

3.76E-15

Neuropathy

 

5.38E-12

Amyotrophic lateral sclerosis

 

1.36E-09

Arthritis

 

1.44E-07