The 2.0 version of rSNPBase
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Variant report
Variant
rs6507751
Chromosome Location
chr18:45022645-45022646
allele
C/T
Outlinks
Ensembl
 
UCSC
Chromatin state
Related regulatory elements
Target genes
Other information
TF binding region (count:1)
CpG islands (count:0)
Chromatin interactive region (count:0)
LncRNA region (count:0)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
(count:1 , 50 per page) page:
1
No.
Transcrition factor
Chromosome Location
Cell Line
Cell type
Cell Stage
Matched TF binding sites
1
NRF1
chr18:45022599-45022715
GM12878
blood:
n/a
n/a
No data
No data
No data
No data
No data
Variant related genes
Relation type
ENSG00000261307
TF binding region
Extended variants information (count: 7 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:7)
rs_ID
r
2
[population]
rs1434502
0.82[ASN][1000 genomes]
rs16954994
1.00[JPT][hapmap]
rs55881359
0.86[EUR][1000 genomes]
rs62097086
0.88[ASN][1000 genomes]
rs6507752
1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6507753
0.85[YRI][hapmap]
rs9963812
0.90[ASN][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