Variant report

Variant	rs10932262
Chromosome Location	chr2:209361037-209361038
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10175430	0.91[ASN][1000 genomes]
rs1057392	0.81[ASN][1000 genomes]
rs11682951	0.84[ASN][1000 genomes]
rs11688433	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11696050	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12105866	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1370374	0.92[ASN][1000 genomes]
rs2014411	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2061013	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2364127	0.81[ASN][1000 genomes]
rs34242215	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36089579	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3820900	0.81[ASN][1000 genomes]
rs3820904	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4675768	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4675770	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4675772	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6726003	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6754577	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7575183	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7604108	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs879707	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209355200-209366000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:209360000-209361200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr2:209360200-209361200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr2:209360200-209361200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr2:209360200-209361400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr2:209360200-209361600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:209360400-209361200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:209360800-209361200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:209361000-209361400	Enhancers	Stomach Mucosa	stomach
10	chr2:209361000-209361600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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