Variant report

Variant	rs6769893
Chromosome Location	chr3:135570030-135570031
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11916990	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1401543	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1519261	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17195888	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17196014	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17196097	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17249203	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1878993	1.00[ASN][1000 genomes]
rs2176666	1.00[ASN][1000 genomes]
rs2895793	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34629706	1.00[ASN][1000 genomes]
rs56382648	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56818259	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57895104	1.00[ASN][1000 genomes]
rs60349283	1.00[ASN][1000 genomes]
rs60545022	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61789012	1.00[ASN][1000 genomes]
rs61789017	1.00[ASN][1000 genomes]
rs61789025	1.00[ASN][1000 genomes]
rs61789026	1.00[ASN][1000 genomes]
rs61790390	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790400	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790401	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790403	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790404	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790457	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790458	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790459	1.00[ASN][1000 genomes]
rs61791710	1.00[ASN][1000 genomes]
rs6414336	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6762218	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6765327	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6769033	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6786217	1.00[ASN][1000 genomes]
rs6802942	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs72977660	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73863014	1.00[ASN][1000 genomes]
rs73863035	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7618257	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7635010	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs908827	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs980210	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9865234	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460860	chr3:135107678-135769006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv591829	chr3:135107678-135769006	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv829732	chr3:135561706-135756840	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135568600-135571000	Enhancers	HSMM	muscle
2	chr3:135569200-135571200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:135569400-135570600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr3:135569400-135571000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:135569600-135570600	Enhancers	Osteobl	bone
6	chr3:135569800-135571000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:135570000-135570800	Enhancers	NH-A	brain
8	chr3:135570000-135571200	Enhancers	HSMMtube	muscle
9	chr3:135570000-135571400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:135570000-135572000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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