The 2.0 version of rSNPBase
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Variant report
Variant
rs17093384
Chromosome Location
chr10:117388634-117388635
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: 13 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:13)
rs_ID
r
2
[population]
rs10509991
0.82[YRI][hapmap]
rs11197282
0.85[YRI][hapmap]
rs1336116
0.88[YRI][hapmap]
rs1536648
0.82[YRI][hapmap]
rs1572402
0.81[YRI][hapmap]
rs17093239
1.00[YRI][hapmap]
rs17093257
1.00[YRI][hapmap]
rs2960684
1.00[EUR][1000 genomes]
rs3858323
0.81[YRI][hapmap]
rs3981279
1.00[EUR][1000 genomes]
rs7068521
0.88[YRI][hapmap]
rs73377564
1.00[EUR][1000 genomes]
rs74158236
1.00[EUR][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