Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11751066	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16884715	0.85[AMR][1000 genomes]
rs16884731	0.85[AMR][1000 genomes]
rs16884733	0.85[AMR][1000 genomes]
rs16884746	0.85[AMR][1000 genomes]
rs16884854	0.82[EUR][1000 genomes]
rs1830595	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3846756	0.85[AMR][1000 genomes]
rs41367946	0.81[AMR][1000 genomes]
rs4385272	0.85[AMR][1000 genomes]
rs4441922	0.85[AMR][1000 genomes]
rs55766784	1.00[AFR][1000 genomes]
rs56168999	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56206543	0.85[AMR][1000 genomes]
rs71555263	1.00[AFR][1000 genomes]
rs72958951	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72958964	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs72958991	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72960912	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72960934	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72969239	0.85[AMR][1000 genomes]
rs72969247	0.85[AMR][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	nsv886167	chr6:75102625-75175449	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	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	chr6:75165600-75168400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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