Variant report

Variant	rs17097841
Chromosome Location	chr1:76462641-76462642
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs11162053	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11162066	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12064158	0.93[ASN][1000 genomes]
rs12091251	0.90[AFR][1000 genomes]
rs12095069	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12402230	0.81[ASN][1000 genomes]
rs12402347	0.97[ASN][1000 genomes]
rs12405994	0.97[ASN][1000 genomes]
rs12408897	0.97[ASN][1000 genomes]
rs12410724	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1251531	0.90[ASN][1000 genomes]
rs1251539	0.92[ASN][1000 genomes]
rs1251550	0.90[ASN][1000 genomes]
rs1251551	0.90[ASN][1000 genomes]
rs1251556	0.92[ASN][1000 genomes]
rs1251560	0.93[ASN][1000 genomes]
rs1251579	0.84[ASN][1000 genomes]
rs1251580	0.84[ASN][1000 genomes]
rs1251581	0.81[ASN][1000 genomes]
rs1251587	0.81[ASN][1000 genomes]
rs1251588	0.84[ASN][1000 genomes]
rs1251591	0.83[ASN][1000 genomes]
rs1251594	0.83[ASN][1000 genomes]
rs1340684	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1361487	0.95[ASN][1000 genomes]
rs1417402	0.97[ASN][1000 genomes]
rs1438175	0.94[ASN][1000 genomes]
rs1438176	1.00[ASN][1000 genomes]
rs1658737	0.90[ASN][1000 genomes]
rs17097821	1.00[ASN][1000 genomes]
rs17097836	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17097837	1.00[ASN][1000 genomes]
rs17097863	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17097864	1.00[ASN][1000 genomes]
rs17097867	0.99[ASN][1000 genomes]
rs1770876	0.90[ASN][1000 genomes]
rs1796799	0.90[ASN][1000 genomes]
rs1873894	0.83[ASN][1000 genomes]
rs1890967	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1938321	0.96[ASN][1000 genomes]
rs1938322	0.90[ASN][1000 genomes]
rs1938323	1.00[ASN][1000 genomes]
rs2066213	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2792664	0.90[ASN][1000 genomes]
rs34574524	1.00[ASN][1000 genomes]
rs3920847	0.97[ASN][1000 genomes]
rs4949619	1.00[ASN][1000 genomes]
rs4949681	0.83[ASN][1000 genomes]
rs4949685	1.00[ASN][1000 genomes]
rs58722308	0.89[ASN][1000 genomes]
rs7418941	0.97[ASN][1000 genomes]
rs7521538	0.89[ASN][1000 genomes]
rs7524665	0.83[ASN][1000 genomes]
rs931506	0.83[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	nsv998499	chr1:76361784-76598712	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr1:76458200-76466600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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