Variant report

Variant	rs16946937
Chromosome Location	chr13:92677816-92677817
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1409501	1.00[EUR][1000 genomes]
rs1409502	1.00[EUR][1000 genomes]
rs1411743	1.00[EUR][1000 genomes]
rs56906091	1.00[EUR][1000 genomes]
rs58772509	1.00[EUR][1000 genomes]
rs58841974	1.00[EUR][1000 genomes]
rs61049774	1.00[EUR][1000 genomes]
rs7336333	1.00[EUR][1000 genomes]
rs73607673	1.00[AMR][1000 genomes]
rs73607679	1.00[AMR][1000 genomes]
rs73607684	1.00[AMR][1000 genomes]
rs73607687	1.00[AMR][1000 genomes]
rs73607696	1.00[AMR][1000 genomes]
rs73620031	1.00[EUR][1000 genomes]
rs73622795	1.00[EUR][1000 genomes]
rs73623542	1.00[EUR][1000 genomes]
rs73624838	1.00[EUR][1000 genomes]
rs7990014	1.00[EUR][1000 genomes]
rs7997781	1.00[EUR][1000 genomes]
rs9583968	1.00[AMR][1000 genomes]
rs9589367	1.00[AMR][1000 genomes]
rs9589404	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9589405	1.00[EUR][1000 genomes]
rs9589408	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9589421	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3378326	chr13:92445514-92816367	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv562722	chr13:92607374-92733984	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv900887	chr13:92651148-92745416	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv900888	chr13:92651148-92748938	Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv900889	chr13:92651148-92772499	Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv900890	chr13:92651148-92808689	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1049238	chr13:92667284-92717880	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv900891	chr13:92668623-92757118	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv900892	chr13:92671868-92745416	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv900893	chr13:92671868-92748938	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv900894	chr13:92671868-92772499	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 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	chr13:92677800-92680600	Enhancers	Fetal Lung	lung

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