Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1587697	0.99[ASN][1000 genomes]
rs164646	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1831430	0.86[ASN][1000 genomes]
rs2484137	0.87[ASN][1000 genomes]
rs2497359	1.00[ASN][1000 genomes]
rs2497360	0.87[ASN][1000 genomes]
rs2497362	0.87[ASN][1000 genomes]
rs2653915	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2782484	0.84[ASN][1000 genomes]
rs352238	0.99[ASN][1000 genomes]
rs352239	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs352242	0.99[ASN][1000 genomes]
rs352245	0.99[ASN][1000 genomes]
rs352246	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs352247	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs352249	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4884853	0.80[ASN][1000 genomes]
rs664401	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67866903	0.86[ASN][1000 genomes]
rs681108	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7317328	1.00[ASN][1000 genomes]
rs949627	0.87[ASN][1000 genomes]
rs9572178	0.87[ASN][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	esv3333426	chr13:70035651-70037749	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70031600-70037000	Enhancers	Brain Germinal Matrix	brain
2	chr13:70036400-70037000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr13:70036800-70037200	Enhancers	HUES6 Cell Line	embryonic stem cell

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