Variant report

Variant	rs11013356
Chromosome Location	chr10:23553075-23553076
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10741026	0.85[AMR][1000 genomes]
rs10764397	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10764398	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10828415	0.93[AMR][1000 genomes]
rs10828419	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10828421	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10828422	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10828423	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10828430	0.89[AMR][1000 genomes]
rs10828431	0.89[AMR][1000 genomes]
rs11013364	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11013386	0.80[ASN][1000 genomes]
rs11013397	0.89[AMR][1000 genomes]
rs11013404	0.89[AMR][1000 genomes]
rs11013412	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11813971	0.86[ASN][1000 genomes]
rs12246990	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12571348	0.98[ASN][1000 genomes]
rs3891382	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4144623	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4258280	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4359107	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4382803	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4433485	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4626975	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4747453	0.93[AMR][1000 genomes]
rs4747455	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4747461	0.80[ASN][1000 genomes]
rs4747466	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4748844	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4748850	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4748866	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4748877	0.86[AMR][1000 genomes]
rs61629455	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7907909	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7919530	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[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	nsv831810	chr10:23445647-23605270	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv466834	chr10:23482635-23623523	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv550213	chr10:23482635-23623523	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr10:23551400-23553400	Weak transcription	Pancreas	Pancrea

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