Variant report

Variant	rs67231683
Chromosome Location	chr3:60863373-60863374
allele	CA/TG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10048949	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13067776	0.86[EUR][1000 genomes]
rs13068391	0.80[EUR][1000 genomes]
rs1447913	0.86[EUR][1000 genomes]
rs1447914	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34412028	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34686536	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34700535	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35744933	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs67192280	0.84[EUR][1000 genomes]
rs6769544	0.86[EUR][1000 genomes]
rs6772360	0.92[EUR][1000 genomes]
rs6772719	0.86[EUR][1000 genomes]
rs6772800	0.84[EUR][1000 genomes]
rs6780515	0.86[EUR][1000 genomes]
rs6783370	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6785030	0.86[EUR][1000 genomes]
rs6785032	0.84[EUR][1000 genomes]
rs6785095	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6787793	0.86[EUR][1000 genomes]
rs6787911	0.86[EUR][1000 genomes]
rs6788110	0.85[EUR][1000 genomes]
rs6791272	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6793385	0.86[EUR][1000 genomes]
rs6793580	0.86[EUR][1000 genomes]
rs6796455	0.86[EUR][1000 genomes]
rs6803394	0.85[EUR][1000 genomes]
rs6804167	0.86[EUR][1000 genomes]
rs73097803	0.81[EUR][1000 genomes]
rs7622729	0.85[EUR][1000 genomes]
rs7627303	0.86[EUR][1000 genomes]
rs7636351	0.85[EUR][1000 genomes]
rs7643970	0.85[EUR][1000 genomes]
rs7644380	0.85[EUR][1000 genomes]
rs7649286	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9754605	0.85[EUR][1000 genomes]
rs9755687	0.86[EUR][1000 genomes]
rs9758127	0.85[EUR][1000 genomes]
rs9827591	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9834435	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9849318	0.86[EUR][1000 genomes]
rs9849474	0.86[EUR][1000 genomes]
rs9849492	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9869424	0.86[EUR][1000 genomes]
rs9870639	0.85[EUR][1000 genomes]
rs9870642	0.85[EUR][1000 genomes]
rs9870929	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534038	chr3:60781917-60993082	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2757872	chr3:60781943-61019003	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2759152	chr3:60781943-61220809	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60862400-60863400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:60862800-60863400	Enhancers	Esophagus	oesophagus
3	chr3:60863000-60863400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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