Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12632090	0.94[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1620446	0.86[JPT][hapmap]
rs1623091	0.81[CEU][hapmap]
rs1716709	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs1716714	0.86[JPT][hapmap]
rs1716718	0.86[JPT][hapmap]
rs1716739	0.86[JPT][hapmap]
rs1735440	0.86[JPT][hapmap]
rs1735443	0.86[JPT][hapmap]
rs1735448	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs1735467	0.85[JPT][hapmap]
rs2682930	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2682931	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2682952	0.90[EUR][1000 genomes]
rs2855998	0.86[JPT][hapmap];0.91[EUR][1000 genomes]
rs2856056	0.81[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap];0.90[ASN][1000 genomes]
rs2856057	0.81[CEU][hapmap]
rs2856058	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2856060	1.00[ASN][1000 genomes]
rs2856067	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2856068	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs986687	0.86[JPT][hapmap]

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	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv999828	chr3:60537384-60785274	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60630800-60639400	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr3:60632800-60637600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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