Variant report

Variant	rs73437567
Chromosome Location	chr11:26171916-26171917
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11820372	0.81[AFR][1000 genomes]
rs56695031	0.88[AFR][1000 genomes]
rs60118133	1.00[AMR][1000 genomes]
rs60444535	1.00[AMR][1000 genomes]
rs60804007	1.00[AMR][1000 genomes]
rs61142566	1.00[AMR][1000 genomes]
rs73429405	1.00[AMR][1000 genomes]
rs73433493	1.00[AMR][1000 genomes]
rs73435421	1.00[AMR][1000 genomes]
rs73435469	1.00[AMR][1000 genomes]
rs73435470	1.00[AMR][1000 genomes]
rs73435474	1.00[AMR][1000 genomes]
rs73435493	1.00[AMR][1000 genomes]
rs73435497	1.00[AMR][1000 genomes]
rs73435500	1.00[AMR][1000 genomes]
rs73437503	1.00[AMR][1000 genomes]
rs73437513	1.00[AMR][1000 genomes]
rs73437515	1.00[AMR][1000 genomes]
rs73437521	1.00[AMR][1000 genomes]
rs73437543	1.00[AMR][1000 genomes]
rs73437546	1.00[AMR][1000 genomes]
rs73437579	0.90[AFR][1000 genomes]
rs73439644	0.90[AFR][1000 genomes]
rs73439645	0.90[AFR][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	nsv832094	chr11:26130733-26292782	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr11:26171400-26172000	Enhancers	Placenta	Placenta

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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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