Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1156764	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11938789	0.92[EUR][1000 genomes]
rs1364837	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1425332	0.91[EUR][1000 genomes]
rs1425335	0.88[EUR][1000 genomes]
rs1863290	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2194858	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28549829	0.83[EUR][1000 genomes]
rs6448036	0.82[AFR][1000 genomes]
rs6448037	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6448038	0.88[EUR][1000 genomes]
rs6821318	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6842655	0.91[EUR][1000 genomes]
rs7437801	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7657718	0.83[EUR][1000 genomes]
rs7672506	0.92[EUR][1000 genomes]
rs7679197	0.91[EUR][1000 genomes]
rs7679226	0.91[EUR][1000 genomes]
rs7679871	0.82[EUR][1000 genomes]
rs7687837	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9291424	0.91[EUR][1000 genomes]
rs929961	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs964613	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv878749	chr4:21189870-21236883	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
5	nsv1002610	chr4:21192993-21261812	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	n/a	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	chr4:21208400-21210400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:21208400-21211400	Weak transcription	HUVEC	blood vessel

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