Variant report

Variant	rs467458
Chromosome Location	chr3:161104027-161104028
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:161097507..161100487-chr3:161101328..161104049,2	K562	blood:
2	chr3:161102931..161104858-chr3:161108932..161110703,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11710086	0.83[ASN][1000 genomes]
rs11710916	0.82[ASN][1000 genomes]
rs11713185	0.86[ASN][1000 genomes]
rs1349352	0.83[ASN][1000 genomes]
rs163137	0.97[EUR][1000 genomes]
rs16832246	0.86[ASN][1000 genomes]
rs16832279	0.83[ASN][1000 genomes]
rs1811483	0.82[ASN][1000 genomes]
rs1839491	0.83[ASN][1000 genomes]
rs2061804	0.93[ASN][1000 genomes]
rs336550	1.00[EUR][1000 genomes]
rs34727114	0.81[ASN][1000 genomes]
rs374501	0.95[AMR][1000 genomes]
rs393076	0.95[AMR][1000 genomes]
rs456137	0.98[AMR][1000 genomes]
rs456331	0.98[AMR][1000 genomes]
rs456882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs458175	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs458344	0.98[AMR][1000 genomes]
rs459565	0.98[AMR][1000 genomes]
rs459592	0.96[AMR][1000 genomes]
rs459923	0.98[AMR][1000 genomes]
rs460013	0.98[AMR][1000 genomes]
rs460176	0.98[AMR][1000 genomes]
rs460950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs460957	0.95[AMR][1000 genomes]
rs460987	0.98[AMR][1000 genomes]
rs463630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs463890	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs465539	0.98[AMR][1000 genomes]
rs465964	0.98[AMR][1000 genomes]
rs466119	0.98[AMR][1000 genomes]
rs466971	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs467353	0.98[AMR][1000 genomes]
rs67077657	0.81[ASN][1000 genomes]
rs73021449	0.83[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	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
3	nsv829772	chr3:161047817-161202554	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
4	nsv877710	chr3:161087857-161245414	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 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	chr3:161102800-161106200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr3:161103200-161105600	Enhancers	Stomach Mucosa	stomach
3	chr3:161103200-161105800	Enhancers	HepG2	liver
4	chr3:161103800-161108200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr3:161104000-161104400	Enhancers	Monocytes-CD14+_RO01746	blood

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