The 2.0 version of rSNPBase
Home
Search
Document
What's New
Tutorial
Data Content
Download
Feedback
About Us
Variant report
Variant
rs7905992
Chromosome Location
chr10:117244091-117244092
allele
A/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: 8 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:8)
rs_ID
r
2
[population]
rs11197225
0.91[ASW][hapmap];0.91[LWK][hapmap];0.90[YRI][hapmap]
rs11197257
0.94[YRI][hapmap]
rs12250436
0.90[YRI][hapmap]
rs12257381
0.90[YRI][hapmap]
rs12260136
0.90[YRI][hapmap]
rs6585334
0.91[ASW][hapmap];0.83[LWK][hapmap];0.90[YRI][hapmap];0.89[AFR][1000 genomes]
rs7096605
0.89[YRI][hapmap]
rs7100292
0.91[ASW][hapmap];0.95[LWK][hapmap];0.90[YRI][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