Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11265174	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11265186	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.94[ASN][1000 genomes]
rs11265187	1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.94[ASN][1000 genomes]
rs11265193	1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.94[ASN][1000 genomes]
rs12045356	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12118628	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs12131860	0.94[ASN][1000 genomes]
rs12145616	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs12410729	0.90[ASN][1000 genomes]
rs2427824	1.00[YRI][hapmap]
rs2427825	1.00[YRI][hapmap]
rs2427828	1.00[YRI][hapmap]
rs2494260	1.00[YRI][hapmap]
rs2494261	1.00[YRI][hapmap]
rs2494263	1.00[YRI][hapmap]
rs2494265	1.00[YRI][hapmap]
rs2511212	1.00[YRI][hapmap]
rs4128725	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs4269772	0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4326616	0.88[ASN][1000 genomes]
rs4656237	0.90[ASN][1000 genomes]
rs4656821	0.94[ASN][1000 genomes]
rs4656826	0.89[ASN][1000 genomes]
rs9782926	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872487	chr1:159196765-159342439	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv872488	chr1:159218266-159336948	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3451967	chr1:159299928-159322549	Enhancers Weak transcription	TF binding region lncRNA	1 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	chr1:159311600-159312800	Enhancers	Primary monocytes fromperipheralblood	blood

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