Variant report

Variant	rs73326698
Chromosome Location	chr12:57265861-57265862
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11171953	1.00[EUR][1000 genomes]
rs11171963	1.00[EUR][1000 genomes]
rs11171964	1.00[EUR][1000 genomes]
rs11171969	1.00[EUR][1000 genomes]
rs11172028	1.00[EUR][1000 genomes]
rs11172032	1.00[EUR][1000 genomes]
rs11172040	1.00[EUR][1000 genomes]
rs11172041	1.00[EUR][1000 genomes]
rs11514185	1.00[EUR][1000 genomes]
rs12299402	1.00[EUR][1000 genomes]
rs12300453	1.00[EUR][1000 genomes]
rs12302242	1.00[EUR][1000 genomes]
rs12306275	1.00[EUR][1000 genomes]
rs12317052	1.00[EUR][1000 genomes]
rs12318649	1.00[EUR][1000 genomes]
rs55935220	1.00[EUR][1000 genomes]
rs57115078	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58416798	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61633783	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73326629	1.00[EUR][1000 genomes]
rs73326643	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73326652	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73326663	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73326665	1.00[EUR][1000 genomes]
rs73326670	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73326673	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73326688	1.00[EUR][1000 genomes]
rs73326690	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73326692	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73326697	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73337089	1.00[EUR][1000 genomes]
rs73337095	1.00[EUR][1000 genomes]
rs73337101	1.00[EUR][1000 genomes]
rs73338912	1.00[EUR][1000 genomes]
rs74093933	1.00[EUR][1000 genomes]
rs74093937	1.00[EUR][1000 genomes]
rs74093946	1.00[EUR][1000 genomes]
rs74093947	1.00[EUR][1000 genomes]
rs9919706	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9919771	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9919774	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040850	chr12:57055011-57679209	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57265400-57270000	Weak transcription	Liver	Liver
2	chr12:57265800-57267600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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