Variant report

Variant	rs59857460
Chromosome Location	chr3:51892880-51892881
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1857800	0.88[ASN][1000 genomes]
rs1983106	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2007607	0.88[ASN][1000 genomes]
rs2089224	0.88[ASN][1000 genomes]
rs2102297	0.83[ASN][1000 genomes]
rs28451928	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs28799908	0.80[ASN][1000 genomes]
rs4280629	0.83[ASN][1000 genomes]
rs4295162	0.83[ASN][1000 genomes]
rs4687602	0.83[ASN][1000 genomes]
rs55804132	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs55886133	0.80[ASN][1000 genomes]
rs55894445	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs56222927	0.88[ASN][1000 genomes]
rs56285190	0.80[ASN][1000 genomes]
rs56662100	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs56998832	0.80[ASN][1000 genomes]
rs57184058	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs57269235	0.80[ASN][1000 genomes]
rs57407585	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs58800810	0.80[ASN][1000 genomes]
rs58929916	0.80[ASN][1000 genomes]
rs58932899	0.83[ASN][1000 genomes]
rs59215394	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs60818362	0.80[ASN][1000 genomes]
rs61015325	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs61257131	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6446041	0.83[ASN][1000 genomes]
rs6763197	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6782139	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6786848	0.82[AMR][1000 genomes]
rs6795223	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6795953	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6798914	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73834762	0.82[AMR][1000 genomes]
rs73834763	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73834764	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73834765	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73834766	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73838706	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs73838710	0.88[ASN][1000 genomes]
rs73838711	0.88[ASN][1000 genomes]
rs7627992	0.88[ASN][1000 genomes]
rs7644969	0.88[ASN][1000 genomes]
rs9831886	0.80[ASN][1000 genomes]
rs9856660	0.83[ASN][1000 genomes]
rs986539	0.88[ASN][1000 genomes]
rs9867413	0.80[ASN][1000 genomes]
rs9875459	0.83[ASN][1000 genomes]
rs9876690	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014464	chr3:51220151-51909780	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv520211	chr3:51772347-52166147	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv1012847	chr3:51811062-52056727	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
4	nsv536571	chr3:51811062-52056727	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
5	nsv1001350	chr3:51860817-51899966	Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51892000-51893800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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