Variant report

Variant	rs1452206
Chromosome Location	chr3:56233022-56233023
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs13323783	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13324556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1452207	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1519030	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1519031	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17056727	0.85[EUR][1000 genomes]
rs28397662	0.90[EUR][1000 genomes]
rs28407987	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28496913	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28583826	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28655135	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28689027	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28766049	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28780379	0.90[EUR][1000 genomes]
rs28829645	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28888991	0.85[EUR][1000 genomes]
rs58152327	0.85[EUR][1000 genomes]
rs59002596	0.90[EUR][1000 genomes]
rs6445782	0.90[EUR][1000 genomes]
rs73832601	0.90[EUR][1000 genomes]
rs9810412	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9815714	0.90[EUR][1000 genomes]
rs9816050	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9818484	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9821284	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9824691	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9834432	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9834759	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9840027	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9842348	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9843455	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9844377	0.95[EUR][1000 genomes]
rs9844806	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9859491	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9865282	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9867542	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9867636	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9878055	0.90[EUR][1000 genomes]
rs9879781	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9880997	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv1009709	chr3:56000827-56294945	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:56230400-56239400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:56230800-56235000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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