Variant report

Variant	rs722958
Chromosome Location	chr5:116170962-116170963
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10035572	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10051070	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10051209	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10053269	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10053279	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10069564	0.92[ASN][1000 genomes]
rs10073924	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1035861	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10463687	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10463688	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10478313	0.83[AMR][1000 genomes]
rs11241403	0.97[ASN][1000 genomes]
rs11956132	0.82[AMR][1000 genomes]
rs12515978	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12517201	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12519375	0.83[AMR][1000 genomes]
rs12521549	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13162142	0.84[ASN][1000 genomes]
rs13163078	0.93[ASN][1000 genomes]
rs13175939	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1366157	0.86[ASN][1000 genomes]
rs1366158	0.96[ASN][1000 genomes]
rs1366159	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1428007	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1544742	0.94[ASN][1000 genomes]
rs1863966	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs26664	0.87[ASN][1000 genomes]
rs27514	0.89[ASN][1000 genomes]
rs2900099	1.00[ASN][1000 genomes]
rs2913598	0.80[ASN][1000 genomes]
rs4920937	0.98[ASN][1000 genomes]
rs6867756	0.81[EUR][1000 genomes]
rs6870730	0.96[ASN][1000 genomes]
rs6896154	0.96[ASN][1000 genomes]
rs7705356	0.94[ASN][1000 genomes]
rs7705508	0.94[ASN][1000 genomes]
rs7710040	0.94[ASN][1000 genomes]
rs7710088	0.94[ASN][1000 genomes]
rs9942388	0.90[ASN][1000 genomes]
rs999415	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116170400-116171000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr5:116170600-116171000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr5:116170600-116171000	Enhancers	HepG2	liver
4	chr5:116170600-116171200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr5:116170800-116171200	Enhancers	HUES64 Cell Line	embryonic stem cell

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