Variant report

Variant	rs1035861
Chromosome Location	chr5:116170317-116170318
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10035572	0.97[ASN][1000 genomes]
rs10051070	0.99[ASN][1000 genomes]
rs10051209	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10053269	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10053279	1.00[ASN][1000 genomes]
rs10069564	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10463687	0.97[ASN][1000 genomes]
rs10463688	0.97[ASN][1000 genomes]
rs10478313	0.81[EUR][1000 genomes]
rs11241403	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11956132	0.80[EUR][1000 genomes]
rs12515978	0.92[ASN][1000 genomes]
rs12517201	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12519375	0.81[EUR][1000 genomes]
rs13162142	0.84[ASN][1000 genomes]
rs13163078	0.93[ASN][1000 genomes]
rs13175939	0.96[ASN][1000 genomes]
rs1366157	0.86[ASN][1000 genomes]
rs1366158	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1366159	0.96[ASN][1000 genomes]
rs1544742	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs26664	0.87[ASN][1000 genomes]
rs27514	0.89[ASN][1000 genomes]
rs2900099	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913598	0.80[ASN][1000 genomes]
rs4920937	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6870730	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6896154	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs722958	1.00[ASN][1000 genomes]
rs7705356	0.94[ASN][1000 genomes]
rs7705508	0.94[ASN][1000 genomes]
rs7710040	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7710088	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9942388	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]

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	nsv830456	chr5:115969066-116170718	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv527974	chr5:115987168-116303678	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv462403	chr5:115994775-116284378	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv599485	chr5:115994775-116284378	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1030056	chr5:116008971-116278725	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1033140	chr5:116035131-116314673	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1027701	chr5:116138286-116185586	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116158400-116170600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:116161400-116170400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr5:116161400-116170600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr5:116166200-116170600	Weak transcription	HepG2	liver
5	chr5:116166400-116170600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr5:116170200-116170600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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