Variant report

Variant	rs16957345
Chromosome Location	chr16:82475662-82475663
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1019958	0.84[ASN][1000 genomes]
rs1073330	0.86[ASN][1000 genomes]
rs11862988	0.81[EUR][1000 genomes]
rs11863613	0.81[EUR][1000 genomes]
rs11863973	0.81[EUR][1000 genomes]
rs1424051	0.95[ASN][1000 genomes]
rs1424052	0.95[ASN][1000 genomes]
rs1424053	0.95[ASN][1000 genomes]
rs1593129	0.88[ASN][1000 genomes]
rs16957377	0.81[EUR][1000 genomes]
rs16957380	0.81[EUR][1000 genomes]
rs16957404	0.81[EUR][1000 genomes]
rs16957411	0.81[EUR][1000 genomes]
rs16957416	0.81[EUR][1000 genomes]
rs16957435	0.81[EUR][1000 genomes]
rs16957439	0.81[EUR][1000 genomes]
rs1962868	0.84[ASN][1000 genomes]
rs3843714	0.81[ASN][1000 genomes]
rs3843715	0.81[ASN][1000 genomes]
rs3843717	0.81[ASN][1000 genomes]
rs3848291	0.81[ASN][1000 genomes]
rs3848292	0.81[ASN][1000 genomes]
rs4060645	0.81[ASN][1000 genomes]
rs4783018	0.81[EUR][1000 genomes]
rs4783020	0.81[EUR][1000 genomes]
rs4783042	0.81[EUR][1000 genomes]
rs73591640	0.81[EUR][1000 genomes]
rs73591641	0.81[EUR][1000 genomes]
rs73591650	0.81[EUR][1000 genomes]
rs73591655	0.81[EUR][1000 genomes]
rs73591657	0.81[EUR][1000 genomes]
rs73591659	0.81[EUR][1000 genomes]
rs73591663	0.81[EUR][1000 genomes]
rs73591672	0.81[EUR][1000 genomes]
rs8048101	0.81[ASN][1000 genomes]
rs8064207	0.80[ASN][1000 genomes]
rs929877	0.84[ASN][1000 genomes]
rs9806957	0.81[ASN][1000 genomes]
rs9888867	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9888928	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9889105	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9889106	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9889113	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9889114	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9927644	0.80[ASN][1000 genomes]
rs9931044	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9936929	0.80[ASN][1000 genomes]
rs9938533	0.84[EUR][1000 genomes]
rs9939482	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532598	chr16:82034475-82738733	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv532599	chr16:82074439-82926863	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv573367	chr16:82140561-83040846	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	nsv1065896	chr16:82213517-82731994	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1057341	chr16:82363800-83198907	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
6	nsv542997	chr16:82363800-83198907	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 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	chr16:82473200-82476000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr16:82475600-82476800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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