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Variant report
Variant
rs73484606
Chromosome Location
chr6:70320271-70320272
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:3)
LncRNA region (count:0)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
No data
No data
(count:3 , 50 per page) page:
1
No.
Distal block
Cell Line
Cell type
Cell Stage
1
chr6:70318773..70320387-chr6:70325810..70327423,2
K562
blood:
2
chr6:70318527..70321655-chr6:70329910..70332211,3
K562
blood:
3
chr6:70320140..70323088-chr6:70342951..70345928,2
MCF-7
breast:
No data
No data
No data
Variant related genes
Relation type
ENSG00000265362
Chromatin interaction
Extended variants information (count: 4 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:3)
rs_ID
r
2
[population]
rs58052158
0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470413
1.00[AMR][1000 genomes]
rs73484608
0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
No.
Variant name
Chromosome position
Chromatin state
Related regulatory elements
Target genes
Extended variants
Associated traits
1
nsv1022847
chr6:70300521-70337899
Enhancers Bivalent Enhancer Weak transcription Active TSS
TF binding regionChromatin interactive region
3 gene(s)
inside rSNPs
diseases
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