Variant report

Variant	rs9595659
Chromosome Location	chr13:47987485-47987486
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 135 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:130)

rs_ID	r²[population]
rs10219892	0.92[EUR][1000 genomes]
rs10219965	0.88[EUR][1000 genomes]
rs10220186	0.92[EUR][1000 genomes]
rs10220209	0.88[EUR][1000 genomes]
rs10220222	0.88[EUR][1000 genomes]
rs11841086	0.88[EUR][1000 genomes]
rs11841823	0.88[EUR][1000 genomes]
rs12385894	0.92[EUR][1000 genomes]
rs1326480	0.80[EUR][1000 genomes]
rs13378192	0.92[EUR][1000 genomes]
rs13378386	0.92[EUR][1000 genomes]
rs13378925	0.92[EUR][1000 genomes]
rs13379023	0.85[EUR][1000 genomes]
rs1340345	0.92[EUR][1000 genomes]
rs1340346	0.92[EUR][1000 genomes]
rs1361457	0.88[EUR][1000 genomes]
rs1417197	0.92[EUR][1000 genomes]
rs1538798	0.90[EUR][1000 genomes]
rs1538800	0.92[EUR][1000 genomes]
rs1819681	0.88[EUR][1000 genomes]
rs2153448	0.88[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes]
rs2478310	0.85[EUR][1000 genomes]
rs2478311	0.85[EUR][1000 genomes]
rs2478338	0.85[EUR][1000 genomes]
rs2478339	0.85[EUR][1000 genomes]
rs2478340	0.85[EUR][1000 genomes]
rs2478341	0.85[EUR][1000 genomes]
rs2486999	0.83[EUR][1000 genomes]
rs2487000	0.88[EUR][1000 genomes]
rs2487007	0.88[EUR][1000 genomes]
rs2503448	0.85[EUR][1000 genomes]
rs2503449	0.85[EUR][1000 genomes]
rs2503450	0.85[EUR][1000 genomes]
rs2503454	0.85[EUR][1000 genomes]
rs4296164	0.92[EUR][1000 genomes]
rs4366617	0.88[EUR][1000 genomes]
rs4411407	0.92[EUR][1000 genomes]
rs4429188	0.88[EUR][1000 genomes]
rs4525393	0.92[EUR][1000 genomes]
rs4525394	0.92[EUR][1000 genomes]
rs4570735	0.88[EUR][1000 genomes]
rs4575434	0.92[EUR][1000 genomes]
rs58200007	0.88[EUR][1000 genomes]
rs6561381	0.88[EUR][1000 genomes]
rs73180354	0.92[EUR][1000 genomes]
rs73180356	0.92[EUR][1000 genomes]
rs73180359	0.92[EUR][1000 genomes]
rs73180360	0.92[EUR][1000 genomes]
rs73180361	0.92[EUR][1000 genomes]
rs73180362	0.92[EUR][1000 genomes]
rs73180363	0.92[EUR][1000 genomes]
rs73180365	0.92[EUR][1000 genomes]
rs73180367	0.92[EUR][1000 genomes]
rs73180372	0.92[EUR][1000 genomes]
rs73180373	0.92[EUR][1000 genomes]
rs73180374	0.92[EUR][1000 genomes]
rs73180375	0.92[EUR][1000 genomes]
rs73180376	0.92[EUR][1000 genomes]
rs73180378	0.92[EUR][1000 genomes]
rs73180379	0.92[EUR][1000 genomes]
rs73180380	0.92[EUR][1000 genomes]
rs73180382	0.92[EUR][1000 genomes]
rs73180383	0.92[EUR][1000 genomes]
rs73180384	0.92[EUR][1000 genomes]
rs73180385	0.92[EUR][1000 genomes]
rs73180386	0.92[EUR][1000 genomes]
rs73180387	0.92[EUR][1000 genomes]
rs73180388	0.92[EUR][1000 genomes]
rs73180391	0.92[EUR][1000 genomes]
rs73180392	0.92[EUR][1000 genomes]
rs73180393	0.92[EUR][1000 genomes]
rs73180394	0.92[EUR][1000 genomes]
rs73180395	0.92[EUR][1000 genomes]
rs73180397	0.92[EUR][1000 genomes]
rs73180398	0.92[EUR][1000 genomes]
rs73180399	0.92[EUR][1000 genomes]
rs73180400	0.92[EUR][1000 genomes]
rs73182203	0.92[EUR][1000 genomes]
rs73182204	0.92[EUR][1000 genomes]
rs73182205	0.92[EUR][1000 genomes]
rs73182207	0.92[EUR][1000 genomes]
rs73182236	0.92[EUR][1000 genomes]
rs73182238	0.92[EUR][1000 genomes]
rs73182239	0.92[EUR][1000 genomes]
rs73182274	0.92[EUR][1000 genomes]
rs73182276	0.92[EUR][1000 genomes]
rs73182277	0.92[EUR][1000 genomes]
rs73182278	0.92[EUR][1000 genomes]
rs73183869	0.85[EUR][1000 genomes]
rs7319491	0.92[EUR][1000 genomes]
rs9316297	0.92[EUR][1000 genomes]
rs9316300	0.92[EUR][1000 genomes]
rs9316301	0.92[EUR][1000 genomes]
rs9316303	0.88[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes]
rs9316304	0.88[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes]
rs9316305	1.00[JPT][hapmap];0.88[EUR][1000 genomes]
rs9316306	0.88[EUR][1000 genomes]
rs9534646	0.92[EUR][1000 genomes]
rs9534647	0.92[EUR][1000 genomes]
rs9534648	0.92[EUR][1000 genomes]
rs9534649	0.92[EUR][1000 genomes]
rs9567866	0.88[EUR][1000 genomes]
rs9591038	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9591039	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9591041	0.92[EUR][1000 genomes]
rs9591050	0.92[EUR][1000 genomes]
rs9591051	0.80[EUR][1000 genomes]
rs9591056	0.92[EUR][1000 genomes]
rs9591057	0.88[EUR][1000 genomes]
rs9595660	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9595662	0.92[EUR][1000 genomes]
rs9595666	0.92[EUR][1000 genomes]
rs9595667	0.92[EUR][1000 genomes]
rs9595668	0.92[EUR][1000 genomes]
rs9595671	0.92[EUR][1000 genomes]
rs9595672	0.92[EUR][1000 genomes]
rs9595673	0.92[EUR][1000 genomes]
rs9595674	0.92[EUR][1000 genomes]
rs9595675	0.92[EUR][1000 genomes]
rs9595687	0.92[EUR][1000 genomes]
rs9595688	0.92[EUR][1000 genomes]
rs9595691	0.92[EUR][1000 genomes]
rs9595709	0.92[EUR][1000 genomes]
rs9595712	0.88[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes]
rs9595713	0.88[EUR][1000 genomes]
rs9595714	0.88[EUR][1000 genomes]
rs9595716	0.88[EUR][1000 genomes]
rs9652163	0.92[EUR][1000 genomes]
rs9943957	0.92[EUR][1000 genomes]
rs997708	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	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3394678	chr13:47678184-48039379	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3450125	chr13:47919050-48236684	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv455879	chr13:47919611-48190106	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv561588	chr13:47943829-48190106	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr13:47983400-47990600	Weak transcription	NHDF-Ad	bronchial
2	chr13:47985000-47988600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr13:47987200-47987600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:47987400-47987600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr13:47987400-47989800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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