Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10932374	0.87[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12467225	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12468497	0.82[AMR][1000 genomes]
rs12471583	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12472934	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13431425	0.95[JPT][hapmap]
rs1595064	0.87[JPT][hapmap]
rs1595066	0.86[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs16845990	0.87[JPT][hapmap]
rs16846013	0.82[CHD][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.87[ASN][1000 genomes]
rs16846048	0.91[JPT][hapmap]
rs1836734	0.88[ASN][1000 genomes]
rs1836735	0.89[ASN][1000 genomes]
rs1836737	0.80[AMR][1000 genomes]
rs1971801	0.90[ASN][1000 genomes]
rs1971802	0.92[ASN][1000 genomes]
rs2887992	0.91[ASN][1000 genomes]
rs3791687	0.82[ASN][1000 genomes]
rs3791691	0.95[JPT][hapmap]
rs3791696	0.86[JPT][hapmap]
rs4673613	0.95[JPT][hapmap]
rs4673614	0.90[JPT][hapmap]
rs60598560	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60650708	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62180134	0.93[ASN][1000 genomes]
rs62180135	0.93[ASN][1000 genomes]
rs6712652	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs6749560	1.00[JPT][hapmap];0.88[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	nsv834522	chr2:212066442-212225328	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv834523	chr2:212163236-212331393	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
3	nsv584313	chr2:212176967-212224689	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv875776	chr2:212196908-212264818	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212214200-212223000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr2:212214200-212232000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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