Variant report

Variant	rs7808200
Chromosome Location	chr7:79680943-79680944
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10272435	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10278055	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1034721	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10486917	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10486920	0.82[ASN][1000 genomes]
rs12668303	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12669805	0.91[ASN][1000 genomes]
rs12673179	0.82[ASN][1000 genomes]
rs12673496	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12673899	0.84[ASN][1000 genomes]
rs17153215	0.92[EUR][1000 genomes]
rs17153306	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17153363	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17153389	0.81[ASN][1000 genomes]
rs17153392	0.84[ASN][1000 genomes]
rs2013085	0.84[ASN][1000 genomes]
rs28607619	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs41488346	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4604374	0.92[EUR][1000 genomes]
rs57112658	0.92[EUR][1000 genomes]
rs58310336	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60238764	0.96[ASN][1000 genomes]
rs61364846	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62460661	0.92[EUR][1000 genomes]
rs62460662	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62460688	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62460690	1.00[EUR][1000 genomes]
rs62460691	1.00[EUR][1000 genomes]
rs62460693	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62460694	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62460695	0.82[EUR][1000 genomes]
rs62460697	0.84[ASN][1000 genomes]
rs62461710	0.92[EUR][1000 genomes]
rs62461731	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62461732	1.00[EUR][1000 genomes]
rs62461734	1.00[EUR][1000 genomes]
rs6964183	0.91[ASN][1000 genomes]
rs7798365	0.96[ASN][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	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv607676	chr7:79636682-79687844	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv818527	chr7:79636682-79687844	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv607677	chr7:79636682-79693050	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv470344	chr7:79659914-79701003	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv607678	chr7:79665817-79726578	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3446832	chr7:79679866-79682014	Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3393711	chr7:79680266-79681514	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	chr7:79678200-79683400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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