Variant report

Variant	rs13243402
Chromosome Location	chr7:121456510-121456511
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1014171	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10238474	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10238868	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10246475	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11766572	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11766594	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11766616	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11768615	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11983105	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12111892	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12535478	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12540905	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12666526	0.81[AMR][1000 genomes]
rs13231796	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2024249	0.81[AMR][1000 genomes]
rs2052131	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2052132	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2052134	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2109764	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2215572	0.81[AMR][1000 genomes]
rs2402589	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2402590	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3757549	0.81[AMR][1000 genomes]
rs4731038	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs740961	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs740962	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs740963	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7802916	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7809971	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7811200	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[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	nsv429808	chr7:121384049-121600049	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:121443200-121458800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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