Variant report

Variant	rs73843680
Chromosome Location	chr3:85637417-85637418
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs55747506	1.00[AMR][1000 genomes]
rs55869020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56375545	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57803625	1.00[AMR][1000 genomes]
rs58822298	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60667710	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843608	1.00[AMR][1000 genomes]
rs73843625	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843628	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843629	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843632	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843661	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843682	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843686	1.00[AMR][1000 genomes]
rs73843689	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73843696	1.00[AFR][1000 genomes]
rs73845485	1.00[AMR][1000 genomes]
rs73845605	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845610	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845611	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845632	1.00[AMR][1000 genomes]
rs73845634	1.00[AMR][1000 genomes]
rs73845639	1.00[AMR][1000 genomes]
rs73845663	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1002238	chr3:85357855-85719373	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
3	nsv536619	chr3:85357855-85719373	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
4	nsv590905	chr3:85438564-85797093	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv998829	chr3:85449960-85641099	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv536622	chr3:85449960-85641099	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv526621	chr3:85470642-85667683	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1009927	chr3:85497666-85669155	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1010541	chr3:85505839-85870597	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv536625	chr3:85505839-85870597	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1006360	chr3:85597755-85683081	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv536629	chr3:85597755-85683081	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1011376	chr3:85599411-85657771	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv590907	chr3:85619451-85694987	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv877101	chr3:85619451-85710336	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85634400-85640800	Weak transcription	Brain Anterior Caudate	brain
2	chr3:85635600-85637800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:85636200-85637800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:85637200-85637600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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