Variant report

Variant	rs12543265
Chromosome Location	chr8:39012173-39012174
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10088458	0.90[EUR][1000 genomes]
rs10088794	0.90[EUR][1000 genomes]
rs10094572	0.90[EUR][1000 genomes]
rs10095244	0.92[EUR][1000 genomes]
rs10095787	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10101558	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10101577	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10106195	0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10108700	0.90[EUR][1000 genomes]
rs10110383	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10111607	0.92[EUR][1000 genomes]
rs10448058	0.92[EUR][1000 genomes]
rs10448059	0.92[EUR][1000 genomes]
rs10448062	0.92[EUR][1000 genomes]
rs10808917	0.92[EUR][1000 genomes]
rs11775433	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11775913	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11777233	0.91[EUR][1000 genomes]
rs11780558	0.92[EUR][1000 genomes]
rs11781014	0.92[EUR][1000 genomes]
rs11781030	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11782591	0.85[EUR][1000 genomes]
rs11783079	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11784002	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11784182	0.92[EUR][1000 genomes]
rs11784263	0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11786404	0.90[EUR][1000 genomes]
rs11786558	0.89[EUR][1000 genomes]
rs12155966	0.92[EUR][1000 genomes]
rs12546310	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12549006	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13439327	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13439544	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13439696	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13439859	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28505965	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28773215	0.92[EUR][1000 genomes]
rs28788037	0.85[EUR][1000 genomes]
rs28801793	0.92[EUR][1000 genomes]
rs28812794	0.92[EUR][1000 genomes]
rs28887526	0.86[EUR][1000 genomes]
rs35815552	0.89[EUR][1000 genomes]
rs3886041	0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4133177	0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4133178	0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4349954	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4476977	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4513935	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4537270	0.81[EUR][1000 genomes]
rs4585712	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4587293	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4733982	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4733983	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4733985	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4733988	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4733991	0.91[EUR][1000 genomes]
rs4733992	0.85[EUR][1000 genomes]
rs55716826	0.92[EUR][1000 genomes]
rs55759907	0.84[EUR][1000 genomes]
rs55892966	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55977531	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56018942	0.87[EUR][1000 genomes]
rs56093547	0.84[EUR][1000 genomes]
rs56392075	0.92[EUR][1000 genomes]
rs6474116	0.92[EUR][1000 genomes]
rs6474117	0.91[EUR][1000 genomes]
rs6981906	0.92[EUR][1000 genomes]
rs6992204	0.92[EUR][1000 genomes]
rs6996235	0.92[EUR][1000 genomes]
rs6997278	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7000543	0.92[EUR][1000 genomes]
rs7010584	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7014889	0.92[EUR][1000 genomes]
rs73606707	0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73606713	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73606714	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73606745	0.92[EUR][1000 genomes]
rs73606748	0.92[EUR][1000 genomes]
rs73606767	0.91[EUR][1000 genomes]
rs73606769	0.90[EUR][1000 genomes]
rs73606771	0.90[EUR][1000 genomes]
rs73606773	0.90[EUR][1000 genomes]
rs73606793	0.84[EUR][1000 genomes]
rs7822982	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7826829	0.91[EUR][1000 genomes]
rs7843696	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7843711	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7845676	0.91[EUR][1000 genomes]
rs9298561	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9771995	0.92[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:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12543265	ADAM32	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:10 , 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	chr8:39001600-39015000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:39001800-39013800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:39004000-39014800	Weak transcription	Left Ventricle	heart
5	chr8:39004200-39013600	Weak transcription	Aorta	Aorta
6	chr8:39006200-39018000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr8:39007800-39015200	Weak transcription	Ovary	ovary
8	chr8:39008400-39018600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr8:39008800-39012400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr8:39009400-39012600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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