Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1022855	0.83[CHD][hapmap]
rs10459429	0.80[ASN][1000 genomes]
rs11847615	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12586326	0.81[ASN][1000 genomes]
rs12588452	0.82[ASN][1000 genomes]
rs12588505	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12588829	0.80[ASN][1000 genomes]
rs12885538	0.80[ASN][1000 genomes]
rs12893733	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1471853	0.82[ASN][1000 genomes]
rs1601593	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17112532	0.80[ASN][1000 genomes]
rs1963723	0.83[ASN][1000 genomes]
rs2029183	0.82[ASN][1000 genomes]
rs34606540	0.80[ASN][1000 genomes]
rs34986689	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6572121	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6572124	0.81[ASN][1000 genomes]
rs7150926	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9323054	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	nsv901740	chr14:42386859-42477256	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42454000-42455200	Weak transcription	Primary B cells from cord blood	blood

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