Variant report

Variant	rs6040533
Chromosome Location	chr20:11299883-11299884
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10432740	0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2024623	0.80[ASN][1000 genomes]
rs2207127	0.90[EUR][1000 genomes]
rs2207128	0.90[EUR][1000 genomes]
rs2327372	0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2327373	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2327374	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2327375	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2327376	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2327400	0.95[EUR][1000 genomes]
rs2876223	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35455280	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4522681	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6033099	0.80[ASN][1000 genomes]
rs6033100	0.80[ASN][1000 genomes]
rs6033101	0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6033103	0.89[EUR][1000 genomes]
rs6033104	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6033109	0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6040526	0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6040529	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6040530	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6040531	0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6074280	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6074296	0.89[EUR][1000 genomes]
rs6078124	0.81[ASN][1000 genomes]
rs6078128	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6078129	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6078154	0.90[EUR][1000 genomes]
rs6078155	0.90[EUR][1000 genomes]
rs6078156	0.90[EUR][1000 genomes]
rs6078158	0.89[EUR][1000 genomes]
rs6078160	0.89[EUR][1000 genomes]
rs6104744	0.90[EUR][1000 genomes]
rs6104746	0.90[EUR][1000 genomes]
rs6108913	0.80[ASN][1000 genomes]
rs6108947	0.89[EUR][1000 genomes]
rs6108949	0.90[EUR][1000 genomes]
rs6108950	0.90[EUR][1000 genomes]
rs6134231	0.88[EUR][1000 genomes]
rs6134235	0.89[EUR][1000 genomes]
rs7269125	0.89[EUR][1000 genomes]
rs764354	0.89[EUR][1000 genomes]
rs764355	0.89[EUR][1000 genomes]
rs8119692	0.89[EUR][1000 genomes]
rs982210	0.81[ASN][1000 genomes]
rs991417	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065969	chr20:10850562-11464172	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv544181	chr20:10850562-11464172	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv585415	chr20:11134907-11383327	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv458869	chr20:11271614-11306751	Enhancers Weak transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv585417	chr20:11271614-11306751	Weak transcription Enhancers ZNF genes & repeats	TF binding region lncRNA	1 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	chr20:11298800-11305200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:11299800-11310200	Weak transcription	Pancreas	Pancrea

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