Variant report

Variant	rs6657899
Chromosome Location	chr1:86703902-86703903
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11161778	0.81[EUR][1000 genomes]
rs11161779	1.00[EUR][1000 genomes]
rs11161780	1.00[EUR][1000 genomes]
rs11161781	0.85[EUR][1000 genomes]
rs12081535	1.00[EUR][1000 genomes]
rs12083520	1.00[EUR][1000 genomes]
rs12562271	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs56046090	0.83[EUR][1000 genomes]
rs6576802	1.00[CEU][hapmap];1.00[TSI][hapmap];0.83[EUR][1000 genomes]
rs6576818	0.81[EUR][1000 genomes]
rs6576821	0.81[EUR][1000 genomes]
rs6576823	0.85[EUR][1000 genomes]
rs6656914	1.00[EUR][1000 genomes]
rs6658327	0.81[EUR][1000 genomes]
rs6669015	0.81[EUR][1000 genomes]
rs6695743	0.83[AFR][1000 genomes]
rs7516602	0.83[AFR][1000 genomes]
rs7521740	0.81[EUR][1000 genomes]
rs7540026	0.81[EUR][1000 genomes]
rs7540048	1.00[LWK][hapmap]
rs7546401	0.83[EUR][1000 genomes]
rs7547133	1.00[CEU][hapmap]
rs7553562	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv546722	chr1:86278315-86891073	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1009092	chr1:86532988-86724805	Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv535024	chr1:86532988-86724805	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv830481	chr1:86550274-86737290	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1003838	chr1:86591841-87212231	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv1002541	chr1:86689088-86905902	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86703000-86704600	Enhancers	Fetal Heart	heart
2	chr1:86703400-86704000	Enhancers	Fetal Lung	lung
3	chr1:86703400-86704200	Enhancers	Fetal Stomach	stomach
4	chr1:86703600-86704200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:86703800-86704200	Enhancers	Stomach Smooth Muscle	stomach

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