Variant report

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

rs_ID	r²[population]
rs10011629	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10033352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11945367	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12331701	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12331762	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12498985	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12499252	0.81[EUR][1000 genomes]
rs12499593	0.81[EUR][1000 genomes]
rs12500339	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12501606	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12506963	0.90[EUR][1000 genomes]
rs12508853	0.90[EUR][1000 genomes]
rs17008928	0.81[EUR][1000 genomes]
rs17008930	0.90[EUR][1000 genomes]
rs17008941	0.90[EUR][1000 genomes]
rs17009001	0.81[EUR][1000 genomes]
rs17009089	0.81[EUR][1000 genomes]
rs17009136	0.90[EUR][1000 genomes]
rs28407125	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28464443	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35278497	0.87[ASN][1000 genomes]
rs57893045	0.91[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	nsv1011752	chr4:125708756-125932456	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1001338	chr4:125708756-126103293	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	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	chr4:125904600-125909200	Weak transcription	Right Atrium	heart
2	chr4:125906000-125907200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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