Variant report

Variant	rs4461996
Chromosome Location	chr9:17700650-17700651
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10116499	1.00[EUR][1000 genomes]
rs4634756	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56036751	1.00[EUR][1000 genomes]
rs56224609	1.00[EUR][1000 genomes]
rs58362676	1.00[EUR][1000 genomes]
rs6475182	1.00[EUR][1000 genomes]
rs727112	1.00[EUR][1000 genomes]
rs73412768	1.00[EUR][1000 genomes]
rs73641997	1.00[AMR][1000 genomes]
rs73642207	1.00[EUR][1000 genomes]
rs73642208	1.00[EUR][1000 genomes]
rs7860584	1.00[EUR][1000 genomes]
rs9406693	1.00[EUR][1000 genomes]
rs9406694	1.00[EUR][1000 genomes]
rs9406696	1.00[EUR][1000 genomes]
rs9406728	1.00[EUR][1000 genomes]
rs9406735	1.00[EUR][1000 genomes]
rs9407833	1.00[EUR][1000 genomes]
rs9407873	1.00[EUR][1000 genomes]
rs9407884	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv613693	chr9:17147191-17710407	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	nsv471287	chr9:17165698-17708814	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv466269	chr9:17165698-17710407	Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv1016971	chr9:17648242-17720176	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	nsv1021022	chr9:17649360-17723730	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv892675	chr9:17694823-17790526	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv466279	chr9:17699981-17726581	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
8	nsv613705	chr9:17699981-17726581	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17699800-17701400	Enhancers	Pancreatic Islets	Pancreatic Islet

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