Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11128176	0.83[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs11128179	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11918342	0.81[ASN][1000 genomes]
rs11929694	0.81[ASN][1000 genomes]
rs12490416	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs12634194	0.81[ASN][1000 genomes]
rs13096169	0.83[ASN][1000 genomes]
rs1491607	0.81[ASN][1000 genomes]
rs1491609	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17790790	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1873566	0.81[ASN][1000 genomes]
rs4491863	0.83[ASN][1000 genomes]
rs4572735	0.82[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4638930	0.88[ASN][1000 genomes]
rs55732253	0.84[ASN][1000 genomes]
rs56196000	0.81[ASN][1000 genomes]
rs56322472	0.81[ASN][1000 genomes]
rs56333904	0.81[ASN][1000 genomes]
rs62256300	0.83[ASN][1000 genomes]
rs6796357	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7431027	0.88[ASN][1000 genomes]
rs7650600	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9849440	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9871358	0.96[CEU][hapmap];0.96[EUR][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	nsv999046	chr3:70549472-70576944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70570200-70576000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr3:70570200-70580800	Weak transcription	H9 Cell Line	embryonic stem cell

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