Variant report

Variant	rs73041327
Chromosome Location	chr2:185391474-185391475
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10206367	1.00[EUR][1000 genomes]
rs11891366	1.00[EUR][1000 genomes]
rs11898500	1.00[EUR][1000 genomes]
rs13384922	1.00[EUR][1000 genomes]
rs13417933	1.00[EUR][1000 genomes]
rs13431559	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2053563	1.00[EUR][1000 genomes]
rs359883	1.00[EUR][1000 genomes]
rs359897	1.00[EUR][1000 genomes]
rs384591	1.00[EUR][1000 genomes]
rs406498	1.00[EUR][1000 genomes]
rs56797758	1.00[EUR][1000 genomes]
rs59038604	1.00[EUR][1000 genomes]
rs61400218	1.00[EUR][1000 genomes]
rs6760206	1.00[EUR][1000 genomes]
rs73041324	1.00[EUR][1000 genomes]
rs73978033	1.00[EUR][1000 genomes]
rs73978034	1.00[EUR][1000 genomes]
rs73978036	1.00[EUR][1000 genomes]
rs73978037	1.00[EUR][1000 genomes]
rs73978039	1.00[EUR][1000 genomes]
rs73978042	1.00[EUR][1000 genomes]
rs73978079	1.00[EUR][1000 genomes]
rs7579459	1.00[EUR][1000 genomes]
rs7601869	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875497	chr2:185134237-185474770	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv875510	chr2:185296258-185400303	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv875511	chr2:185300641-185400303	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv875512	chr2:185300641-185474770	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv532412	chr2:185347334-186108701	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	esv3409319	chr2:185386495-185412533	Enhancers ZNF genes & repeats Weak transcription Active TSS	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	chr2:185388600-185393000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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