Variant report

Variant	rs9811886
Chromosome Location	chr3:179986047-179986048
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10212464	1.00[AMR][1000 genomes]
rs13320177	1.00[AMR][1000 genomes]
rs13325335	1.00[AMR][1000 genomes]
rs60802670	1.00[AMR][1000 genomes]
rs73063387	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73065307	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73065310	1.00[AMR][1000 genomes]
rs73065340	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73065370	1.00[AMR][1000 genomes]
rs9825552	1.00[AMR][1000 genomes]
rs9829129	1.00[AMR][1000 genomes]
rs9835211	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9838957	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9841661	1.00[AMR][1000 genomes]
rs9842402	1.00[AMR][1000 genomes]
rs9861862	1.00[AMR][1000 genomes]
rs9866426	1.00[AMR][1000 genomes]
rs9883551	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv878040	chr3:179823887-180128288	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv997388	chr3:179899279-180172349	Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv536817	chr3:179899279-180172349	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv878041	chr3:179983857-180097855	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179980600-179992400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:179985200-179994800	Weak transcription	Brain Angular Gyrus	brain
3	chr3:179985400-179992600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:179985800-179986400	Enhancers	GM12878-XiMat	blood
5	chr3:179986000-179987200	Enhancers	Dnd41	blood

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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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