Variant report

Variant	rs13412940
Chromosome Location	chr2:124797055-124797056
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10181162	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10196297	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10496627	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1213959	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12470976	1.00[AMR][1000 genomes]
rs12711668	1.00[AMR][1000 genomes]
rs12711669	1.00[AMR][1000 genomes]
rs12711670	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]
rs17010871	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17279639	1.00[JPT][hapmap]
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]
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]
rs4241118	1.00[AMR][1000 genomes]
rs4505528	1.00[AMR][1000 genomes]
rs6731948	1.00[AMR][1000 genomes]
rs6740328	1.00[AMR][1000 genomes]
rs6747933	1.00[AMR][1000 genomes]
rs7567589	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7579069	1.00[AMR][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	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:124796200-124797200	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr2:124796400-124797200	Enhancers	H1 Cell Line	embryonic stem cell
3	chr2:124796400-124797200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr2:124796600-124797200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:124796600-124797200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:124797000-124798600	Enhancers	Pancreatic Islets	Pancreatic Islet

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