Variant report

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

rs_ID	r²[population]
rs13435481	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28727307	0.83[ASN][1000 genomes]
rs4383633	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4593148	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57504424	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs60074415	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60120540	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61471044	0.89[EUR][1000 genomes]
rs72615864	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs72615865	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs72615878	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72615884	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72615885	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72615886	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72615895	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72616304	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72616306	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72616307	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72616359	0.89[EUR][1000 genomes]
rs72616370	0.89[EUR][1000 genomes]
rs72616371	0.89[EUR][1000 genomes]
rs72616381	0.89[EUR][1000 genomes]
rs72616384	0.89[EUR][1000 genomes]
rs7685810	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428770	chr4:130692631-130863832	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1019516	chr4:130754819-130976202	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130805000-130805400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:130805200-130805600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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