Variant report
Variant |
rs148925535 |
Chromosome Location |
chr13:61869145-61869146 |
allele |
A/C
|
Outlinks |
Ensembl
 
UCSC
|
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
No. |
Variant name |
Chromosome position |
Chromatin state |
Related regulatory elements |
Target genes |
Extended variants |
Associated traits |
1 |
nsv518287 |
chr13:61867724-61873379 |
Active TSS Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
diseases
|
Chromatin state (count:1 , 50 per page) page:
1
No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
1 |
chr13:61869000-61870200 |
Enhancers |
Pancreatic Islets |
Pancreatic Islet
|
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