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Variant report
Variant
rs7604266
Chromosome Location
chr2:141324913-141324914
allele
A/C
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:1)
LncRNA region (count:0)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
No data
No data
(count:1 , 50 per page) page:
1
No.
Distal block
Cell Line
Cell type
Cell Stage
1
chr2:141323740..141325865-chr2:141332665..141335542,2
MCF-7
breast:
No data
No data
No data
No data
Extended variants information (count: 7 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:5)
rs_ID
r
2
[population]
rs1905922
1.00[YRI][hapmap]
rs522410
0.83[YRI][hapmap]
rs535615
0.82[YRI][hapmap]
rs6430924
1.00[YRI][hapmap]
rs7565092
1.00[YRI][hapmap]
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
No.
Variant name
Chromosome position
Chromatin state
Related regulatory elements
Target genes
Extended variants
Associated traits
1
nsv583192
chr2:141310721-141350100
Enhancers Weak transcription
Chromatin interactive regionmiRNA
n/a
inside rSNPs
n/a
2
nsv459529
chr2:141321160-141350100
Enhancers Weak transcription
Chromatin interactive regionmiRNA
n/a
inside rSNPs
n/a
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