Variant report

Variant	rs61320353
Chromosome Location	chr13:62036768-62036769
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs2876810	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4447303	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4468495	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4474590	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4592536	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61601007	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74080845	1.00[AMR][1000 genomes]
rs74080846	1.00[AMR][1000 genomes]
rs74080851	1.00[AMR][1000 genomes]
rs74080852	1.00[AMR][1000 genomes]
rs74080877	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs74080878	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs74081855	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081856	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081857	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081858	0.97[AFR][1000 genomes]
rs74081859	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081866	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081868	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081869	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081870	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081871	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081873	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081875	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081876	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081877	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081878	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081879	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081880	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900245	chr13:61873379-62057698	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv948661	chr13:61906251-62179649	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv2761266	chr13:61928642-62690828	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv832628	chr13:61985540-62153692	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv948810	chr13:62003256-62968196	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	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	chr13:62036400-62037000	Enhancers	Pancreatic Islets	Pancreatic Islet

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