Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1078308	0.86[ASN][1000 genomes]
rs10864049	1.00[ASN][1000 genomes]
rs10864050	1.00[ASN][1000 genomes]
rs11120152	1.00[ASN][1000 genomes]
rs11120153	1.00[ASN][1000 genomes]
rs11120154	1.00[ASN][1000 genomes]
rs1391870	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1532535	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17020842	1.00[CHB][hapmap]
rs2165131	1.00[ASN][1000 genomes]
rs2501457	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs320385	0.94[EUR][1000 genomes]
rs320386	0.94[EUR][1000 genomes]
rs320388	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs320393	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs320422	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs320424	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs320426	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs393105	1.00[CEU][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs401923	1.00[CEU][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4073190	0.88[EUR][1000 genomes]
rs410108	1.00[CEU][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs430997	0.93[EUR][1000 genomes]
rs450826	0.92[CEU][hapmap]
rs4655294	1.00[ASN][1000 genomes]
rs4655295	1.00[ASN][1000 genomes]
rs4655446	1.00[ASN][1000 genomes]
rs4655447	1.00[ASN][1000 genomes]
rs4655448	1.00[ASN][1000 genomes]
rs6682832	0.85[EUR][1000 genomes]
rs920355	1.00[ASN][1000 genomes]
rs920357	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832525	chr1:213580476-213782815	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213697000-213697800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:213697200-213697800	Bivalent Enhancer	Left Ventricle	heart
3	chr1:213697400-213697800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:213697600-213697800	Enhancers	Right Ventricle	heart

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