Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11800181	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11802784	1.00[ASN][1000 genomes]
rs12062568	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12062937	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12079191	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1601235	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4907945	1.00[ASN][1000 genomes]
rs4907946	1.00[ASN][1000 genomes]
rs4907948	1.00[ASN][1000 genomes]
rs4907950	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4908169	1.00[ASN][1000 genomes]
rs56064810	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56140505	1.00[ASN][1000 genomes]
rs56173817	0.84[EUR][1000 genomes]
rs56221742	0.87[EUR][1000 genomes]
rs56807681	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57544888	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60629450	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6660076	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6679807	0.82[AMR][1000 genomes];0.84[EUR][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	nsv870459	chr1:102112168-102166616	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:102146400-102147600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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