Variant report

Variant	rs11840967
Chromosome Location	chr13:61494449-61494450
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1857724	0.95[ASN][1000 genomes]
rs2134867	0.95[ASN][1000 genomes]
rs2274655	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2671872	0.95[ASN][1000 genomes]
rs302892	0.95[ASN][1000 genomes]
rs3884484	0.95[ASN][1000 genomes]
rs4886288	1.00[CHB][hapmap]
rs7328316	0.95[ASN][1000 genomes]
rs9538990	0.95[ASN][1000 genomes]
rs9538992	0.95[ASN][1000 genomes]
rs9598207	0.95[ASN][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	nsv832624	chr13:61383648-61553974	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61494400-61496000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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