Variant report

Variant	rs4733983
Chromosome Location	chr8:39015793-39015794
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10088458	0.91[EUR][1000 genomes]
rs10088794	0.91[EUR][1000 genomes]
rs10094572	0.91[EUR][1000 genomes]
rs10095244	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10095787	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10101558	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10101577	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10106195	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10108700	0.91[EUR][1000 genomes]
rs10110383	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10111607	0.94[EUR][1000 genomes]
rs10448058	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10448059	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10448062	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10808917	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11775433	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11775913	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11777233	0.92[EUR][1000 genomes]
rs11780558	0.94[EUR][1000 genomes]
rs11781014	0.94[EUR][1000 genomes]
rs11781030	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11782591	0.86[EUR][1000 genomes]
rs11783079	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11784002	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11784182	0.94[EUR][1000 genomes]
rs11784263	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11786404	0.91[EUR][1000 genomes]
rs11786558	0.90[EUR][1000 genomes]
rs12155966	0.94[EUR][1000 genomes]
rs12543265	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12546310	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12549006	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13439327	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13439544	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13439696	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13439859	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28505965	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28773215	0.94[EUR][1000 genomes]
rs28788037	0.86[EUR][1000 genomes]
rs28801793	0.94[EUR][1000 genomes]
rs28812794	0.94[EUR][1000 genomes]
rs28887526	0.87[EUR][1000 genomes]
rs35815552	0.90[EUR][1000 genomes]
rs3886041	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4133177	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4133178	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4349954	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4476977	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4513935	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4537270	0.82[EUR][1000 genomes]
rs4585712	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4587293	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4733982	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4733985	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4733988	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4733991	0.92[EUR][1000 genomes]
rs4733992	0.86[EUR][1000 genomes]
rs55716826	0.94[EUR][1000 genomes]
rs55759907	0.85[EUR][1000 genomes]
rs55892966	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55977531	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56018942	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56093547	0.85[EUR][1000 genomes]
rs56392075	0.94[EUR][1000 genomes]
rs6474116	0.93[EUR][1000 genomes]
rs6474117	0.92[EUR][1000 genomes]
rs6981906	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6992204	0.94[EUR][1000 genomes]
rs6996235	0.94[EUR][1000 genomes]
rs6997278	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7000543	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7010584	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7014889	0.93[EUR][1000 genomes]
rs73606707	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73606713	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73606714	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73606745	0.94[EUR][1000 genomes]
rs73606748	0.94[EUR][1000 genomes]
rs73606767	0.92[EUR][1000 genomes]
rs73606769	0.91[EUR][1000 genomes]
rs73606771	0.91[EUR][1000 genomes]
rs73606773	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73606793	0.85[EUR][1000 genomes]
rs7822982	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7826829	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7843696	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7843711	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7845676	0.92[EUR][1000 genomes]
rs9298561	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9771995	0.94[EUR][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	nsv1021581	chr8:38934014-39043954	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv1015907	chr8:38967169-39718559	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv539550	chr8:38967169-39718559	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1027443	chr8:38993423-39181079	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv539551	chr8:38993423-39181079	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4733983	ADAM32	cis	Adipose Subcutaneous	GTEx
rs4733983	ADAM32	cis	Esophagus Muscularis	GTEx

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:38971200-39036400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:39006200-39018000	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr8:39008400-39018600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr8:39013600-39015800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:39013800-39018600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:39015000-39016200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:39015200-39015800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:39015200-39016200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:39015200-39016200	ZNF genes & repeats	Aorta	Aorta
10	chr8:39015200-39016200	ZNF genes & repeats	Ovary	ovary
11	chr8:39015400-39016000	ZNF genes & repeats	Adipose Nuclei	Adipose
12	chr8:39015600-39018200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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