Variant report

Variant	rs62296663
Chromosome Location	chr4:19457866-19457867
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10000100	0.84[EUR][1000 genomes]
rs10027425	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10222776	0.92[EUR][1000 genomes]
rs10440273	0.84[EUR][1000 genomes]
rs28427059	0.84[EUR][1000 genomes]
rs28582056	0.84[EUR][1000 genomes]
rs28595109	0.84[EUR][1000 genomes]
rs28630700	0.84[EUR][1000 genomes]
rs28665147	0.84[EUR][1000 genomes]
rs28715168	0.84[EUR][1000 genomes]
rs57920411	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58006599	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs60408185	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296407	0.84[EUR][1000 genomes]
rs62296409	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62296410	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62296411	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62296413	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296415	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296419	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296446	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296448	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296450	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296451	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296453	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296454	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296662	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296664	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296703	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296704	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296705	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296706	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296708	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62296710	0.90[EUR][1000 genomes]
rs62296737	0.84[EUR][1000 genomes]
rs62296738	0.84[EUR][1000 genomes]
rs62298660	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298661	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298662	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298686	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298687	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298717	0.88[AMR][1000 genomes]
rs62298730	0.97[EUR][1000 genomes]
rs62298731	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298732	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298734	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298735	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298738	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62298767	0.84[EUR][1000 genomes]
rs62298770	0.89[EUR][1000 genomes]
rs62298816	0.84[EUR][1000 genomes]
rs62298824	0.84[EUR][1000 genomes]
rs62298825	0.84[EUR][1000 genomes]
rs62299860	0.84[EUR][1000 genomes]
rs62300184	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62300186	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73800842	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73800847	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73800857	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73800865	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73800869	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv593785	chr4:19092157-19521956	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv878732	chr4:19172031-19660947	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv878733	chr4:19335464-19928602	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr4:19456800-19458800	Active TSS	Placenta	Placenta

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