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Variant report
Variant
rs10487220
Chromosome Location
chr7:104272864-104272865
allele
C/T
Outlinks
Ensembl
 
UCSC
Chromatin state
Related regulatory elements
Target genes
Other information
TF binding region (count:0)
CpG islands (count:0)
Chromatin interactive region (count:0)
LncRNA region (count:0)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
No data
No data
No data
No data
No data
No data
No data
Extended variants information (count: 9 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:9)
rs_ID
r
2
[population]
rs12667073
1.00[ASW][hapmap]
rs2216243
0.86[CEU][hapmap]
rs2216244
0.80[MEX][hapmap]
rs2891730
0.80[MEX][hapmap]
rs4367471
1.00[ASW][hapmap]
rs4730031
0.80[MEX][hapmap]
rs4730032
0.92[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap]
rs9640680
0.86[CEU][hapmap]
rs9640682
0.90[CEU][hapmap];0.83[GIH][hapmap];0.90[MEX][hapmap];0.88[TSI][hapmap]
No data
Chromatin state (count:0 , 50 per page) page:
No data
Quick Search:
Input of quick search could be:
dbSNP/dbVar ID:
rs12345
/
nsv7879
a single nucleotide as 0-based coordinates:
chr1:12345
chromosomal regions:
chr1:12345-34567
what's new
New variant types
New dimension of annotation
New regulatory manner
More detailed annotation on variant overlapped TFBS
More extended data
New search manner
Quick links