Variant report

Variant	rs9881586
Chromosome Location	chr3:34589478-34589479
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11129600	0.91[ASN][1000 genomes]
rs12632484	0.87[EUR][1000 genomes]
rs12636370	0.86[EUR][1000 genomes]
rs13353395	0.87[EUR][1000 genomes]
rs28668619	0.87[EUR][1000 genomes]
rs34234856	0.80[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs60041320	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6765600	0.87[EUR][1000 genomes]
rs6773245	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6776887	0.87[EUR][1000 genomes]
rs6777100	0.87[EUR][1000 genomes]
rs6788571	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6792099	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs6801572	0.87[EUR][1000 genomes]
rs73060667	0.80[ASN][1000 genomes]
rs9311059	0.92[ASN][1000 genomes]
rs9881051	0.87[EUR][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	nsv1007906	chr3:34466966-34607465	ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 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	chr3:34589200-34589600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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