Variant report

Variant	rs16891947
Chromosome Location	chr6:81237839-81237840
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:81047651..81048631-chr6:81237581..81238534,2	MCF-7	breast:
2	chr16:28172997..28173848-chr6:81237133..81237839,2	MCF-7	breast:

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs11963283	1.00[ASN][1000 genomes]
rs11963932	1.00[ASN][1000 genomes]
rs11966186	1.00[ASN][1000 genomes]
rs11968846	0.89[ASN][1000 genomes]
rs11968922	0.89[ASN][1000 genomes]
rs12332795	1.00[ASN][1000 genomes]
rs12332966	1.00[ASN][1000 genomes]
rs12333205	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12333251	1.00[ASN][1000 genomes]
rs1377977	1.00[ASN][1000 genomes]
rs1377978	1.00[ASN][1000 genomes]
rs16891950	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28380152	0.89[ASN][1000 genomes]
rs28420284	0.83[ASN][1000 genomes]
rs4569928	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs55685719	1.00[ASN][1000 genomes]
rs56180349	1.00[ASN][1000 genomes]
rs57974544	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs58511607	0.92[ASN][1000 genomes]
rs58667188	1.00[ASN][1000 genomes]
rs59084260	1.00[ASN][1000 genomes]
rs60453104	1.00[ASN][1000 genomes]
rs654625	1.00[CHB][hapmap]
rs6902143	0.88[ASN][1000 genomes]
rs6907126	1.00[ASN][1000 genomes]
rs6928662	1.00[ASN][1000 genomes]
rs73473502	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7744624	1.00[ASN][1000 genomes]
rs7745055	1.00[ASN][1000 genomes]
rs7746193	0.88[ASN][1000 genomes]
rs7756619	1.00[ASN][1000 genomes]
rs7761017	1.00[ASN][1000 genomes]
rs7761850	1.00[ASN][1000 genomes]
rs7776114	1.00[ASN][1000 genomes]
rs9443778	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9443782	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9443783	0.92[ASN][1000 genomes]
rs9443784	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9443794	1.00[ASN][1000 genomes]
rs9443795	1.00[ASN][1000 genomes]
rs9443796	1.00[ASN][1000 genomes]
rs9443798	1.00[ASN][1000 genomes]
rs9443803	0.89[ASN][1000 genomes]
rs9449014	0.92[ASN][1000 genomes]
rs9449015	0.92[ASN][1000 genomes]
rs9449016	0.92[ASN][1000 genomes]
rs9449017	0.92[ASN][1000 genomes]
rs9449018	0.92[ASN][1000 genomes]
rs9449019	0.92[ASN][1000 genomes]
rs9449020	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9449021	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9449022	0.88[ASN][1000 genomes]
rs9449023	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9449024	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9449035	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9449040	1.00[ASN][1000 genomes]
rs9449041	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9449044	1.00[ASN][1000 genomes]
rs9449051	1.00[ASN][1000 genomes]
rs9449053	0.96[ASN][1000 genomes]
rs9449054	0.92[ASN][1000 genomes]
rs9449056	1.00[ASN][1000 genomes]
rs9449057	1.00[ASN][1000 genomes]
rs9449062	1.00[ASN][1000 genomes]
rs9449065	1.00[ASN][1000 genomes]
rs9449077	0.96[ASN][1000 genomes]
rs9449078	0.96[ASN][1000 genomes]
rs9449079	0.96[ASN][1000 genomes]
rs9449085	0.92[ASN][1000 genomes]
rs9449086	1.00[ASN][1000 genomes]
rs9449087	1.00[ASN][1000 genomes]
rs9449088	1.00[ASN][1000 genomes]
rs9449092	0.89[ASN][1000 genomes]
rs9449096	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531333	chr6:81042427-81836484	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1019670	chr6:81086504-81569984	ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv915714	chr6:81134888-81366749	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv886311	chr6:81166178-81239971	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv886312	chr6:81166178-81309481	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv886313	chr6:81177227-81239971	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv463908	chr6:81232993-81287675	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv604054	chr6:81232993-81287675	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81233600-81249600	Weak transcription	HSMM	muscle
2	chr6:81234000-81238000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:81234200-81239200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:81234200-81245000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:81234200-81245200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr6:81234200-81249600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:81237000-81238200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:81237000-81238200	Enhancers	Hela-S3	cervix
9	chr6:81237000-81238400	Enhancers	Fetal Intestine Small	intestine
10	chr6:81237200-81238200	Enhancers	Stomach Mucosa	stomach
11	chr6:81237400-81238000	Enhancers	Duodenum Mucosa	Duodenum
12	chr6:81237400-81238200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:81237400-81238200	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr6:81237400-81238400	Enhancers	Fetal Heart	heart
15	chr6:81237600-81238000	Flanking Active TSS	Liver	Liver
16	chr6:81237600-81238000	Weak transcription	Fetal Lung	lung
17	chr6:81237600-81238000	Enhancers	Small Intestine	intestine
18	chr6:81237600-81238000	Flanking Active TSS	HepG2	liver
19	chr6:81237600-81238200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:81237800-81238200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr6:81237800-81238200	Enhancers	Fetal Intestine Large	intestine
22	chr6:81237800-81238200	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr6:81237800-81238200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr6:81237800-81238200	Enhancers	A549	lung
25	chr6:81237800-81238400	Enhancers	Pancreas	Pancrea
26	chr6:81237800-81238800	Enhancers	NHDF-Ad	bronchial

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