Variant report

Variant	rs4858461
Chromosome Location	chr3:22904663-22904664
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1114382	1.00[EUR][1000 genomes]
rs12107605	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12107606	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12108183	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1450304	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1450306	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1450308	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1597451	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1597452	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17012124	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17012167	0.90[ASN][1000 genomes]
rs17012235	0.96[ASN][1000 genomes]
rs2122471	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2122472	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28419496	1.00[EUR][1000 genomes]
rs28864513	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28875337	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4470547	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4858053	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4858453	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4858454	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4858456	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4858459	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858460	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858465	1.00[EUR][1000 genomes]
rs4858466	1.00[EUR][1000 genomes]
rs6767946	0.98[AFR][1000 genomes]
rs6771115	0.83[AFR][1000 genomes]
rs6774861	0.82[AFR][1000 genomes]
rs7624850	1.00[EUR][1000 genomes]
rs7652748	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460477	chr3:22532660-22920246	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv589941	chr3:22532660-22920246	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1014828	chr3:22554271-23033498	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1008306	chr3:22762892-23026548	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22900200-22905600	Weak transcription	Ovary	ovary
2	chr3:22901800-22911600	Weak transcription	Fetal Lung	lung
3	chr3:22904200-22904800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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