Variant report

Variant	rs1023802
Chromosome Location	chr4:95898525-95898526
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs1023800	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1023801	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1023803	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1023804	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11097454	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1160695	1.00[CHB][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12507710	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13128586	0.86[ASN][1000 genomes]
rs13129054	0.86[ASN][1000 genomes]
rs13129062	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13145631	1.00[CHB][hapmap];0.94[AFR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1318972	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1347346	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1434546	0.85[CHB][hapmap]
rs1434548	1.00[CHB][hapmap]
rs1444920	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1444921	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1444923	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1444926	0.82[ASN][1000 genomes]
rs1469336	1.00[CHB][hapmap]
rs1470409	0.82[ASN][1000 genomes]
rs1530459	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1545326	0.85[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs1545327	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.86[YRI][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1545329	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1560909	0.85[CHB][hapmap]
rs1821451	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1822826	0.80[AFR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1838501	1.00[CHB][hapmap];0.82[JPT][hapmap];0.88[YRI][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1867542	1.00[CHB][hapmap];0.88[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1867543	0.83[AMR][1000 genomes]
rs2028761	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2044328	1.00[CHB][hapmap];0.88[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2099996	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2120832	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2865398	1.00[CHB][hapmap]
rs3755874	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3755875	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs3775033	1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap]
rs3775034	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4145993	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs4331783	0.82[ASN][1000 genomes]
rs4397000	0.82[ASN][1000 genomes]
rs4426786	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs4450936	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4588466	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4699825	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4699826	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4699827	0.86[ASN][1000 genomes]
rs4699828	1.00[CHB][hapmap];0.88[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6532520	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6813361	0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6815448	1.00[CHB][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6816059	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6820199	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6836504	1.00[CHB][hapmap];0.88[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6840826	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs6841746	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6843668	1.00[CHB][hapmap];0.88[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6844029	1.00[CHB][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6846665	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6853845	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6855395	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs716190	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.86[ASN][1000 genomes]
rs7665167	1.00[CHB][hapmap]
rs7698787	1.00[CHB][hapmap];0.88[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs920911	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs920912	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs965447	1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.90[ASN][1000 genomes]
rs973887	1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs996659	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9995627	0.85[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932216	chr4:95501261-96109807	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1005816	chr4:95573444-95902704	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv492312	chr4:95823124-96128327	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv997787	chr4:95859839-95934105	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv537190	chr4:95859839-95934105	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95894200-95904800	Weak transcription	Aorta	Aorta
2	chr4:95896400-95901400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:95897000-95898600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:95897000-95898800	Enhancers	Osteobl	bone
5	chr4:95897400-95898600	Enhancers	NHDF-Ad	bronchial
6	chr4:95897600-95898600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr4:95897600-95898600	Enhancers	HSMM	muscle
8	chr4:95898200-95898600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:95898400-95898600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:95898400-95898600	Weak transcription	Ovary	ovary
11	chr4:95898400-95899600	Weak transcription	NH-A	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links