Variant report

Variant	rs7756861
Chromosome Location	chr6:71712667-71712668
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10945292	1.00[AMR][1000 genomes]
rs11965581	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12110901	1.00[EUR][1000 genomes]
rs12111243	1.00[EUR][1000 genomes]
rs12182033	1.00[EUR][1000 genomes]
rs16881007	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55666367	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56131215	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56161362	1.00[EUR][1000 genomes]
rs56192260	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56365444	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59282007	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59358439	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59600420	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60100541	1.00[AMR][1000 genomes]
rs60222660	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60316641	1.00[EUR][1000 genomes]
rs61498740	1.00[EUR][1000 genomes]
rs6907270	1.00[EUR][1000 genomes]
rs6916069	1.00[EUR][1000 genomes]
rs6916241	1.00[EUR][1000 genomes]
rs6917091	1.00[EUR][1000 genomes]
rs6927030	1.00[EUR][1000 genomes]
rs6930158	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73497926	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73497994	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73498002	1.00[EUR][1000 genomes]
rs73498904	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73498909	1.00[EUR][1000 genomes]
rs73499815	1.00[EUR][1000 genomes]
rs73499826	1.00[EUR][1000 genomes]
rs73746981	1.00[AMR][1000 genomes]
rs73746987	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73746995	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73746997	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73749806	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73749809	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7738396	1.00[EUR][1000 genomes]
rs7762477	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7771883	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446299	1.00[EUR][1000 genomes]
rs9455236	1.00[EUR][1000 genomes]
rs9969061	1.00[AMR][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	nsv966627	chr6:71699692-71726851	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	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	chr6:71695600-71716600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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