Variant report

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

rs_ID	r²[population]
rs10736066	0.81[ASN][1000 genomes]
rs1417257	0.81[ASN][1000 genomes]
rs1538832	0.81[ASN][1000 genomes]
rs17347260	0.81[ASN][1000 genomes]
rs17433251	0.81[ASN][1000 genomes]
rs1772181	0.81[ASN][1000 genomes]
rs1772186	0.81[ASN][1000 genomes]
rs1772188	0.81[ASN][1000 genomes]
rs2258946	0.81[ASN][1000 genomes]
rs2421705	0.81[ASN][1000 genomes]
rs2421706	0.81[ASN][1000 genomes]
rs61743258	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61874668	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61874670	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61874701	0.81[ASN][1000 genomes]
rs61876142	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61876145	0.92[EUR][1000 genomes]
rs61876151	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6583792	0.81[ASN][1000 genomes]
rs7089495	0.81[ASN][1000 genomes]
rs72823110	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72823162	0.81[ASN][1000 genomes]
rs7912830	0.81[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	nsv895892	chr10:93432632-93470167	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93454400-93459600	Weak transcription	Liver	Liver

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