Variant report

Variant	rs7212188
Chromosome Location	chr17:67203464-67203465
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1011789	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1024598	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11077396	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11077403	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11077408	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11077414	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1118164	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11654430	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11655199	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11655912	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11658738	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11659119	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11868299	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12451663	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12940557	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12941264	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12943387	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12948396	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12950143	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12951091	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12952984	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1558167	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1974578	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2215149	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2364990	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2364991	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2364992	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4358004	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4968841	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4968842	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4968850	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62082734	0.84[ASN][1000 genomes]
rs7208382	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs721813	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7221183	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7223736	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8064583	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8065924	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8066629	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8067584	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8069791	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8070459	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8071249	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8071373	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8071611	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8073982	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8075377	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8079681	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8080065	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8080693	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9709278	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs981453	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9894644	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9909216	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9910035	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[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	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv470598	chr17:67081830-67212595	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv575930	chr17:67120025-67212031	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv457888	chr17:67149973-67226643	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv575931	chr17:67149973-67226643	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv575932	chr17:67149973-67327806	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv575933	chr17:67153386-67215712	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:67144000-67236000	Weak transcription	Psoas Muscle	Psoas
2	chr17:67160600-67220000	Weak transcription	Fetal Lung	lung
3	chr17:67173400-67230000	Weak transcription	Pancreas	Pancrea
4	chr17:67180600-67209000	Weak transcription	Ovary	ovary
5	chr17:67189600-67208600	Weak transcription	Liver	Liver
6	chr17:67189600-67209000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr17:67189800-67221400	Weak transcription	Right Ventricle	heart
8	chr17:67192600-67219200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr17:67195000-67209600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr17:67198200-67214800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr17:67201600-67215200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr17:67202400-67203600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr17:67202400-67204000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr17:67202600-67204000	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr17:67203200-67203600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr17:67203400-67215000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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