Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10828867	0.99[ASN][1000 genomes]
rs10828868	0.98[ASN][1000 genomes]
rs11014715	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11014719	0.99[ASN][1000 genomes]
rs11527760	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11813354	0.98[ASN][1000 genomes]
rs12781784	0.87[ASN][1000 genomes]
rs2442871	0.85[ASN][1000 genomes]
rs2442872	0.90[ASN][1000 genomes]
rs2442873	0.90[ASN][1000 genomes]
rs2442877	0.88[ASN][1000 genomes]
rs2442878	0.90[ASN][1000 genomes]
rs2442879	0.85[ASN][1000 genomes]
rs2442881	0.90[ASN][1000 genomes]
rs2442882	0.90[ASN][1000 genomes]
rs2442886	0.85[ASN][1000 genomes]
rs2442887	0.85[ASN][1000 genomes]
rs2504197	0.90[ASN][1000 genomes]
rs2504202	0.90[ASN][1000 genomes]
rs2504203	0.90[ASN][1000 genomes]
rs2505423	0.83[ASN][1000 genomes]
rs2505426	0.83[ASN][1000 genomes]
rs2505444	0.90[ASN][1000 genomes]
rs2923025	0.90[ASN][1000 genomes]
rs4749072	0.99[ASN][1000 genomes]
rs4749074	0.90[ASN][1000 genomes]
rs9417445	0.90[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	esv3380301	chr10:26005549-26011700	Enhancers Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26005400-26011800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr10:26009400-26012000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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