Variant report
Variant |
rs200827444 |
Chromosome Location |
chr5:91699541-91699542 |
allele |
C/G
|
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 |
esv7943 |
chr5:91699447-91699646 |
Enhancers
|
n/a
|
n/a
|
inside rSNPs
|
n/a
|
Chromatin state (count:1 , 50 per page) page:
1
No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
1 |
chr5:91698800-91699600 |
Enhancers |
Fetal Heart |
heart
|
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