Variant report

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

rs_ID	r²[population]
rs12894998	0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs177216	0.90[GIH][hapmap]
rs177226	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs177229	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs177232	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs177238	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs177239	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs177243	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1955571	0.88[ASN][1000 genomes]
rs3896379	0.85[ASN][1000 genomes]
rs4903686	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4903687	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4903688	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4903689	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6574416	0.80[ASN][1000 genomes]
rs7146614	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7152858	0.89[ASN][1000 genomes]
rs7153421	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7160437	0.88[ASN][1000 genomes]
rs8005420	0.84[GIH][hapmap]
rs8019668	0.92[ASN][1000 genomes]
rs8021165	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs8022316	0.80[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	nsv902108	chr14:78459047-78541015	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island 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	chr14:78502200-78503200	Enhancers	Brain Germinal Matrix	brain

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