Variant report

Variant	rs58376959
Chromosome Location	chr5:59712428-59712429
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10056638	0.94[ASN][1000 genomes]
rs10073390	0.97[ASN][1000 genomes]
rs10514893	0.85[EUR][1000 genomes]
rs10514894	0.85[EUR][1000 genomes]
rs11745274	0.97[ASN][1000 genomes]
rs11745327	0.97[ASN][1000 genomes]
rs1423471	0.84[EUR][1000 genomes]
rs16877933	0.85[EUR][1000 genomes]
rs16877936	0.85[EUR][1000 genomes]
rs16877964	0.93[EUR][1000 genomes]
rs16877967	0.93[EUR][1000 genomes]
rs16878035	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16878037	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16878086	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16878104	0.89[AMR][1000 genomes]
rs16878106	0.82[EUR][1000 genomes]
rs17326404	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17378750	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1862589	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28460011	0.97[ASN][1000 genomes]
rs28635931	0.97[ASN][1000 genomes]
rs3763059	0.84[EUR][1000 genomes]
rs4090603	0.84[EUR][1000 genomes]
rs55952213	0.89[EUR][1000 genomes]
rs56151644	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56217581	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56247947	0.89[EUR][1000 genomes]
rs56262275	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs57177718	0.89[EUR][1000 genomes]
rs58512371	0.89[EUR][1000 genomes]
rs58594585	0.85[EUR][1000 genomes]
rs58704174	0.89[EUR][1000 genomes]
rs58891299	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59014679	0.89[EUR][1000 genomes]
rs59313902	0.84[EUR][1000 genomes]
rs59576667	0.89[EUR][1000 genomes]
rs59578756	0.89[EUR][1000 genomes]
rs60104228	1.00[EUR][1000 genomes]
rs60962155	0.93[EUR][1000 genomes]
rs61474228	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6864442	0.97[ASN][1000 genomes]
rs6875484	0.93[ASN][1000 genomes]
rs6878429	0.84[EUR][1000 genomes]
rs6881782	0.85[EUR][1000 genomes]
rs6886423	0.93[EUR][1000 genomes]
rs6887545	0.97[ASN][1000 genomes]
rs6887925	0.97[ASN][1000 genomes]
rs6896850	0.97[ASN][1000 genomes]
rs73106781	0.89[EUR][1000 genomes]
rs73106782	0.89[EUR][1000 genomes]
rs73108627	0.89[EUR][1000 genomes]
rs73108631	0.89[EUR][1000 genomes]
rs73759052	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73759053	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73759054	0.97[ASN][1000 genomes]
rs7702188	0.85[EUR][1000 genomes]
rs7723861	0.84[EUR][1000 genomes]
rs7725629	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7737086	0.84[EUR][1000 genomes]
rs9291690	0.99[ASN][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	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv598288	chr5:59627555-60003460	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1015381	chr5:59678425-59772485	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1034331	chr5:59678773-59773467	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1018614	chr5:59708223-59910308	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1033344	chr5:59710033-59773467	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 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	chr5:59695000-59712600	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59696000-59713200	Weak transcription	Aorta	Aorta
3	chr5:59712200-59713000	Enhancers	Primary B cells from peripheral blood	blood
4	chr5:59712400-59713000	Enhancers	GM12878-XiMat	blood
5	chr5:59712400-59716800	Enhancers	HepG2	liver

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