Variant report

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10204261	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12711669	1.00[AMR][1000 genomes]
rs12711670	1.00[AMR][1000 genomes]
rs13382328	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13421371	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1358670	1.00[AMR][1000 genomes]
rs1358671	1.00[AMR][1000 genomes]
rs1358672	1.00[AMR][1000 genomes]
rs1358673	1.00[AMR][1000 genomes]
rs1358674	1.00[AMR][1000 genomes]
rs1358675	1.00[AMR][1000 genomes]
rs1358676	1.00[AMR][1000 genomes]
rs1406659	1.00[AMR][1000 genomes]
rs1529293	1.00[AMR][1000 genomes]
rs1529300	1.00[AMR][1000 genomes]
rs1529302	1.00[AMR][1000 genomes]
rs1529303	1.00[AMR][1000 genomes]
rs1529304	1.00[AMR][1000 genomes]
rs1529305	1.00[AMR][1000 genomes]
rs1540892	1.00[AMR][1000 genomes]
rs1919834	1.00[AMR][1000 genomes]
rs1919845	1.00[AMR][1000 genomes]
rs1919846	1.00[AMR][1000 genomes]
rs1919847	1.00[AMR][1000 genomes]
rs1919848	1.00[AMR][1000 genomes]
rs1919849	1.00[AMR][1000 genomes]
rs2141541	1.00[AMR][1000 genomes]
rs2439004	1.00[AMR][1000 genomes]
rs2565757	1.00[AMR][1000 genomes]
rs2565758	1.00[AMR][1000 genomes]
rs2579822	1.00[AMR][1000 genomes]
rs2699368	1.00[AMR][1000 genomes]
rs2699369	1.00[AMR][1000 genomes]
rs2699370	1.00[AMR][1000 genomes]
rs2699371	1.00[AMR][1000 genomes]
rs2699372	1.00[AMR][1000 genomes]
rs2699373	1.00[AMR][1000 genomes]
rs6740328	1.00[AMR][1000 genomes]
rs6747933	1.00[AMR][1000 genomes]
rs7579069	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874989	chr2:124892592-125176030	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv874990	chr2:125038678-125099924	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	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	chr2:125072600-125073000	Enhancers	Stomach Smooth Muscle	stomach

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