Variant report

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

rs_ID	r²[population]
rs10427172	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11888548	1.00[ASN][1000 genomes]
rs11901831	1.00[ASN][1000 genomes]
rs12619707	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs16846036	1.00[JPT][hapmap]
rs1821661	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1836739	0.86[ASN][1000 genomes]
rs34588906	0.89[ASN][1000 genomes]
rs55985613	0.86[AMR][1000 genomes]
rs56172792	1.00[ASN][1000 genomes]
rs58735954	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59224996	0.93[ASN][1000 genomes]
rs60254210	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66471203	1.00[ASN][1000 genomes]
rs66600814	1.00[ASN][1000 genomes]
rs67103742	0.98[ASN][1000 genomes]
rs72947641	1.00[ASN][1000 genomes]
rs72947669	0.91[ASN][1000 genomes]
rs72947685	0.87[ASN][1000 genomes]
rs73083810	1.00[ASN][1000 genomes]
rs73083812	1.00[ASN][1000 genomes]
rs7571041	0.88[EUR][1000 genomes];1.00[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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