Variant report

Variant	rs16877926
Chromosome Location	chr5:59655640-59655641
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10461373	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10461452	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10461453	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10514890	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10514891	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs10514892	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10514895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12653662	0.90[CEU][hapmap];0.91[EUR][1000 genomes]
rs12656804	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12656836	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12656871	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12659623	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13158470	0.90[EUR][1000 genomes]
rs13158573	0.85[CEU][hapmap];0.90[EUR][1000 genomes]
rs13159724	0.88[CEU][hapmap];0.90[EUR][1000 genomes]
rs13178509	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs13185075	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs16877859	1.00[CEU][hapmap]
rs16877953	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs16877954	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs16877976	0.89[CEU][hapmap]
rs2961774	0.87[CEU][hapmap]
rs34114616	0.94[EUR][1000 genomes]
rs34757284	0.90[EUR][1000 genomes]
rs34762984	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35022567	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35250060	0.90[EUR][1000 genomes]
rs35335033	0.97[ASN][1000 genomes]
rs35813355	0.90[EUR][1000 genomes]
rs35955333	0.89[EUR][1000 genomes]
rs4274945	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4276368	0.86[EUR][1000 genomes]
rs4515249	0.88[CEU][hapmap];0.90[JPT][hapmap];0.86[EUR][1000 genomes]
rs4700373	1.00[CEU][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6869495	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6880937	0.94[EUR][1000 genomes]
rs71628002	0.89[EUR][1000 genomes]
rs71630003	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71630005	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7711621	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs7711707	0.90[EUR][1000 genomes]
rs7718384	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs7731452	0.90[EUR][1000 genomes]
rs7735398	0.90[CEU][hapmap]

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	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv598288	chr5:59627555-60003460	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59647200-59658000	Weak transcription	Hela-S3	cervix
2	chr5:59647200-59694200	Weak transcription	Primary B cells from cord blood	blood
3	chr5:59649400-59668200	Weak transcription	Gastric	stomach
4	chr5:59650400-59657600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr5:59650400-59674800	Weak transcription	Aorta	Aorta
6	chr5:59650800-59657400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr5:59655600-59655800	Enhancers	Rectal Smooth Muscle	rectum

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