Table 4.

Correlation between chromosomal features and integration sites




Carrier

ATL

Human genome, %
No. (%)
P1*
No. (%)
P1*
P2
Total    56   NA   59   NA   NA  
SINES   12.8   3 (5.3)   NS   4 (6.8)   NS   NS  
LINES   20   10 (17.9)   NS   9 (15.3)   NS   NS  
DNA elements   2.8   1 (1.8)   NS   2 (3.4)   NS   NS  
LTR elements   8.3   6 (10.7)   NS   4 (6.8)   NS   NS  
Satellite       
   Alpha satellite   5   11 (19.6)   .0153   2 (3.4)   NS   .0059  
   Beta satellite
 
UN
 
0 (0.0)
 
UN
 
0 (0.0)
 
UN
 
NS
 



Carrier

ATL

Human genome, %
No. (%)
P1*
No. (%)
P1*
P2
Total    56   NA   59   NA   NA  
SINES   12.8   3 (5.3)   NS   4 (6.8)   NS   NS  
LINES   20   10 (17.9)   NS   9 (15.3)   NS   NS  
DNA elements   2.8   1 (1.8)   NS   2 (3.4)   NS   NS  
LTR elements   8.3   6 (10.7)   NS   4 (6.8)   NS   NS  
Satellite       
   Alpha satellite   5   11 (19.6)   .0153   2 (3.4)   NS   .0059  
   Beta satellite
 
UN
 
0 (0.0)
 
UN
 
0 (0.0)
 
UN
 
NS
 

Percentages of repetitive sequences in the human genome were based on Venter et al.18 

NS indicates not significant; UN, unknown; NA, not applicable.

*

P1 shows comparison with genome frequency with the use of Fisher exact test

P2 shows comparison with carrier integration with the use of Fisher exact test

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