Variant report

Variant	rs11529591
Chromosome Location	chr11:16525079-16525080
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1004283	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10500830	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10741698	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10766324	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10766325	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10766327	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832602	0.82[EUR][1000 genomes]
rs10832603	0.82[EUR][1000 genomes]
rs10832604	0.84[EUR][1000 genomes]
rs10832607	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10832609	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10832610	0.87[EUR][1000 genomes]
rs10832616	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10832617	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10832619	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10832620	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10832624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832625	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10832626	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832631	0.87[EUR][1000 genomes]
rs10832632	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10832636	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10832638	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10832644	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10832645	0.87[EUR][1000 genomes]
rs11023932	0.82[EUR][1000 genomes]
rs11023934	0.84[EUR][1000 genomes]
rs11023940	0.84[EUR][1000 genomes]
rs11023942	0.84[EUR][1000 genomes]
rs11023943	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11023947	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11023964	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11023965	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11023969	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11023971	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11023985	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11023990	0.83[EUR][1000 genomes]
rs11023991	0.83[EUR][1000 genomes]
rs11529135	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11605526	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12221729	0.84[EUR][1000 genomes]
rs12221945	0.83[EUR][1000 genomes]
rs12221946	0.83[EUR][1000 genomes]
rs12222249	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12364390	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12418604	0.87[EUR][1000 genomes]
rs12421422	0.83[EUR][1000 genomes]
rs12799024	0.82[ASN][1000 genomes]
rs1393924	0.83[EUR][1000 genomes]
rs1503440	0.82[EUR][1000 genomes]
rs16933105	0.82[EUR][1000 genomes]
rs16933117	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1948824	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2134610	0.84[EUR][1000 genomes]
rs2174164	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs297338	0.81[AMR][1000 genomes]
rs34952258	0.83[EUR][1000 genomes]
rs4132991	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4237714	0.83[EUR][1000 genomes]
rs4259791	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4307685	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4447141	0.81[EUR][1000 genomes]
rs4491181	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4550186	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4756850	0.84[EUR][1000 genomes]
rs4756851	0.83[EUR][1000 genomes]
rs4757397	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4757398	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4757399	0.84[EUR][1000 genomes]
rs4757402	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4757403	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4757410	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4757414	0.83[EUR][1000 genomes]
rs61881805	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61881829	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61881830	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61883215	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61883864	0.81[ASN][1000 genomes]
rs61883867	0.80[EUR][1000 genomes]
rs61883868	0.84[EUR][1000 genomes]
rs7122873	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7483029	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7935820	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7951243	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7951760	0.86[EUR][1000 genomes]
rs9666320	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9704273	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv897016	chr11:16455794-16691743	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr11:16510400-16533000	Weak transcription	Fetal Heart	heart
2	chr11:16520600-16527200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:16524800-16525800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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