Variant report

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

rs_ID	r²[population]
rs10469656	0.89[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12469375	0.89[CEU][hapmap];0.83[CHB][hapmap];0.83[ASN][1000 genomes]
rs12616462	0.89[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12694246	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12694247	0.90[AMR][1000 genomes]
rs1818752	0.88[CEU][hapmap];0.95[AFR][1000 genomes]
rs1829612	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1851175	0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1851176	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1851177	0.89[CEU][hapmap];0.82[JPT][hapmap]
rs1851190	0.89[CEU][hapmap];0.94[EUR][1000 genomes]
rs1851194	1.00[CEU][hapmap];0.81[CHB][hapmap];0.96[EUR][1000 genomes]
rs1851195	0.84[EUR][1000 genomes]
rs1851196	0.86[JPT][hapmap]
rs3863853	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4605309	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4672620	0.89[CEU][hapmap];0.82[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs4673625	1.00[ASN][1000 genomes]
rs7559679	0.93[JPT][hapmap]
rs7565192	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7580963	0.83[ASN][1000 genomes]
rs7593315	0.94[EUR][1000 genomes]
rs7601664	0.89[CEU][hapmap];0.83[CHB][hapmap];0.83[ASN][1000 genomes]
rs9288436	0.85[JPT][hapmap]

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	nsv584321	chr2:212446818-212511895	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2754366	chr2:212470494-212541494	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
3	nsv460070	chr2:212492764-212541377	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
4	nsv584322	chr2:212492764-212541377	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region	1 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	chr2:212467400-212546800	Weak transcription	Aorta	Aorta
2	chr2:212488400-212502800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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