Variant report

Variant	rs35338484
Chromosome Location	chr16:52261654-52261655
allele	A/G
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:26)

rs_ID	r²[population]
rs1080489	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1080490	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11076444	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12149541	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12921318	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12930272	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12930844	0.80[ASN][1000 genomes]
rs1362376	0.80[ASN][1000 genomes]
rs1362382	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1420202	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1420208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16950964	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34764426	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3826196	0.80[ASN][1000 genomes]
rs3859116	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3906325	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4620949	0.81[AFR][1000 genomes]
rs62041398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62041400	0.89[AFR][1000 genomes]
rs62041402	0.86[AFR][1000 genomes]
rs62041403	0.86[AFR][1000 genomes]
rs67253370	0.80[ASN][1000 genomes]
rs67505663	0.81[ASN][1000 genomes]
rs67753568	0.82[ASN][1000 genomes]
rs72792194	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72794118	0.82[ASN][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	nsv492248	chr16:51681902-52456082	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	esv34024	chr16:51878565-52316530	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1058257	chr16:52093549-52271815	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 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	chr16:52260600-52262400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr16:52261200-52263200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr16:52261400-52262400	Weak transcription	Placenta	Placenta
4	chr16:52261600-52262200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr16:52261600-52262200	Enhancers	Fetal Kidney	kidney

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