The 2.0 version of rSNPBase
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Variant report
Variant
rs11822429
Chromosome Location
chr11:76133382-76133383
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:2)
LncRNA region (count:0)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
No data
No data
(count:2 , 50 per page) page:
1
No.
Distal block
Cell Line
Cell type
Cell Stage
1
chr11:76121767..76124244-chr11:76133041..76136016,3
K562
blood:
2
chr11:76132118..76140418-chr11:76149873..76158428,11
K562
blood:
No data
No data
No data
Variant related genes
Relation type
ENSG00000158636
Chromatin interaction
ENSG00000255135
Chromatin interaction
Extended variants information (count: 0)
Associated traits (count: 0)
No data
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