Variant report

Variant	rs73115466
Chromosome Location	chr4:28319890-28319891
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1158230	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1158231	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11935635	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11945645	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11947184	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1391220	1.00[AFR][1000 genomes]
rs16880558	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1846118	0.82[EUR][1000 genomes]
rs34890254	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58224835	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58411582	1.00[AFR][1000 genomes]
rs60588324	0.82[EUR][1000 genomes]
rs6848787	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs73113837	1.00[AFR][1000 genomes]
rs73115468	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117858	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117862	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117864	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117866	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117867	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117869	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117870	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117875	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117878	0.87[EUR][1000 genomes]
rs73117880	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117883	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117887	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117890	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73117891	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73804356	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7677693	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005382	chr4:28157180-28403800	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv878775	chr4:28163856-28473048	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1000514	chr4:28192982-28445194	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv878777	chr4:28208093-28343903	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv878778	chr4:28237783-28343903	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1012210	chr4:28246489-28419673	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv878779	chr4:28264394-28343903	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1010133	chr4:28273244-28642942	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv878780	chr4:28273999-28341254	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1014938	chr4:28277683-28642942	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr4:28316400-28322800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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