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Variant report
Variant
rs16866897
Chromosome Location
chr2:180529886-180529887
allele
A/G
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: 10 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:10)
rs_ID
r
2
[population]
rs16866891
1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs16866893
1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs16866898
1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs16866901
0.97[AFR][1000 genomes]
rs16866916
1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs16866918
1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs55935953
0.83[AFR][1000 genomes]
rs58946184
0.97[AFR][1000 genomes]
rs6722937
1.00[CHB][hapmap]
rs73976035
1.00[AFR][1000 genomes]
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