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Variant report
Variant
rs16922068
Chromosome Location
chr10:22489827-22489828
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:5)
LncRNA region (count:0)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
No data
No data
(count:5 , 50 per page) page:
1
No.
Distal block
Cell Line
Cell type
Cell Stage
1
chr10:22488725..22490375-chr10:22491958..22493892,2
K562
blood:
2
chr10:22290067..22292410-chr10:22489678..22492178,2
K562
blood:
3
chr10:22488920..22491268-chr10:22498235..22500113,2
MCF-7
breast:
4
chr10:22488525..22491217-chr10:22517571..22520488,4
K562
blood:
5
chr10:22488241..22490225-chr10:22491086..22493892,2
K562
blood:
No data
No data
No data
Variant related genes
Relation type
ENSG00000223601
Chromatin interaction
ENSG00000136770
Chromatin interaction
Extended variants information (count: 8 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:8)
rs_ID
r
2
[population]
rs1034023
1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16922091
1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16922110
1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16922114
1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16922142
1.00[AMR][1000 genomes]
rs1926694
1.00[ASN][1000 genomes]
rs1926695
1.00[ASN][1000 genomes]
rs913331
1.00[AMR][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