Variant report

Variant	rs9990084
Chromosome Location	chr3:67831662-67831663
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1599208	1.00[AMR][1000 genomes]
rs17046932	1.00[AMR][1000 genomes]
rs28808348	1.00[AMR][1000 genomes]
rs57420241	1.00[AMR][1000 genomes]
rs58065813	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59042613	1.00[AMR][1000 genomes]
rs59316357	1.00[AMR][1000 genomes]
rs60230188	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60791408	1.00[AMR][1000 genomes]
rs61390227	1.00[AMR][1000 genomes]
rs72919783	1.00[AMR][1000 genomes]
rs72930817	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72930819	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9849582	1.00[AMR][1000 genomes]
rs9856031	1.00[AMR][1000 genomes]
rs9867941	1.00[AMR][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	nsv1002010	chr3:67785913-68312064	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	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	chr3:67831600-67832000	Enhancers	Primary T cells fromperipheralblood	blood
2	chr3:67831600-67832400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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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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