Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs17060966	1.00[EUR][1000 genomes]
rs17061007	1.00[EUR][1000 genomes]
rs2022612	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2327193	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55742557	1.00[EUR][1000 genomes]
rs57075525	1.00[EUR][1000 genomes]
rs58299965	1.00[EUR][1000 genomes]
rs58884491	1.00[EUR][1000 genomes]
rs61085013	1.00[EUR][1000 genomes]
rs6906828	1.00[EUR][1000 genomes]
rs6909873	1.00[EUR][1000 genomes]
rs73543504	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73543507	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73543511	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73543527	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73543545	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73543554	1.00[EUR][1000 genomes]
rs73543593	1.00[EUR][1000 genomes]
rs73545551	1.00[EUR][1000 genomes]
rs73545576	1.00[EUR][1000 genomes]
rs73545600	1.00[EUR][1000 genomes]
rs73547580	1.00[EUR][1000 genomes]
rs73547586	1.00[EUR][1000 genomes]
rs73547600	1.00[EUR][1000 genomes]
rs73779148	1.00[EUR][1000 genomes]
rs9321316	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9483367	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9483368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9493165	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs957535	0.83[AMR][1000 genomes]
rs9885614	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470861	chr6:132291785-132351866	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv886672	chr6:132299748-132349215	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv886673	chr6:132299748-132363507	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv427768	chr6:132300468-132398477	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132326000-132330400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:132326800-132332000	Weak transcription	Aorta	Aorta
3	chr6:132327000-132328600	Weak transcription	HepG2	liver
4	chr6:132327000-132330800	Weak transcription	Stomach Mucosa	stomach
5	chr6:132327200-132328600	Weak transcription	NHDF-Ad	bronchial
6	chr6:132328200-132329600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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