Variant report

Variant	rs12272629
Chromosome Location	chr11:56049318-56049319
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11227762	0.90[AFR][1000 genomes]
rs11824850	0.90[AFR][1000 genomes]
rs12274193	0.90[AFR][1000 genomes]
rs12277630	0.90[AFR][1000 genomes]
rs17541821	0.94[EUR][1000 genomes]
rs17541876	0.94[EUR][1000 genomes]
rs17613345	1.00[EUR][1000 genomes]
rs17627302	0.85[EUR][1000 genomes]
rs55706115	0.94[EUR][1000 genomes]
rs55892403	0.94[EUR][1000 genomes]
rs56077409	0.94[EUR][1000 genomes]
rs61888282	1.00[EUR][1000 genomes]
rs61888286	1.00[EUR][1000 genomes]
rs61888289	1.00[EUR][1000 genomes]
rs61888309	1.00[EUR][1000 genomes]
rs61888312	1.00[EUR][1000 genomes]
rs61888313	1.00[EUR][1000 genomes]
rs61901983	0.85[EUR][1000 genomes]
rs61902021	0.83[EUR][1000 genomes]
rs61902022	0.83[EUR][1000 genomes]
rs61902863	0.83[EUR][1000 genomes]
rs61903478	0.95[EUR][1000 genomes]
rs61903482	0.97[EUR][1000 genomes]
rs61903483	0.97[EUR][1000 genomes]
rs61903484	0.94[EUR][1000 genomes]
rs61903485	0.94[EUR][1000 genomes]
rs61903486	0.94[EUR][1000 genomes]
rs61903487	0.94[EUR][1000 genomes]
rs61903530	0.95[EUR][1000 genomes]
rs61903531	0.95[EUR][1000 genomes]
rs61903536	0.95[EUR][1000 genomes]
rs61903537	0.95[EUR][1000 genomes]
rs61903541	0.95[EUR][1000 genomes]
rs7103598	0.85[EUR][1000 genomes]
rs7106248	0.94[EUR][1000 genomes]
rs7121384	0.94[EUR][1000 genomes]
rs7121385	0.94[EUR][1000 genomes]
rs7124023	0.94[EUR][1000 genomes]
rs7125690	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7126549	0.83[EUR][1000 genomes]
rs716103	1.00[EUR][1000 genomes]
rs716104	1.00[EUR][1000 genomes]
rs7932621	1.00[EUR][1000 genomes]
rs7951134	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7951506	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv975114	chr11:55751535-56124251	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv521440	chr11:55763943-56052521	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv1044859	chr11:55900482-56121727	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv1050024	chr11:55900482-56518943	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
5	nsv497854	chr11:55917298-56537994	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
6	nsv832161	chr11:56046173-56166964	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56047000-56049800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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