Variant report

Variant	rs13338592
Chromosome Location	chr16:71550607-71550608
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs13331092	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13335958	1.00[AMR][1000 genomes]
rs13338643	0.83[AMR][1000 genomes]
rs13339359	0.83[AMR][1000 genomes]
rs16973227	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28436693	1.00[AMR][1000 genomes]
rs28448676	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59475931	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73584836	1.00[AMR][1000 genomes]
rs73589850	1.00[AMR][1000 genomes]
rs8053156	0.83[AMR][1000 genomes]
rs8060811	1.00[AMR][1000 genomes]
rs9921203	0.83[AMR][1000 genomes]
rs9926624	0.83[AMR][1000 genomes]
rs9927547	1.00[AMR][1000 genomes]
rs9927810	1.00[AMR][1000 genomes]
rs9940830	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949461	chr16:71196153-71579711	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv906892	chr16:71526720-71570413	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71549200-71558400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr16:71549800-71551200	Enhancers	Pancreas	Pancrea

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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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